Canonical Allele Identifier: CA16617966
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 423828
ClinVar RCV Id: RCV000478309
dbSNP Id: rs1064796646
MyVariant Identifiers: chr3:g.41275793G>C (hg19) chr3:g.41234302G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.41234302G>C , CM000665.2:g.41234302G>C GRCh38
NC_000003.11:g.41275793G>C , CM000665.1:g.41275793G>C GRCh37
NC_000003.10:g.41250797G>C NCBI36
NG_013302.1:g.39852G>C
NG_013302.2:g.39852G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000349496.11:c.1683+5G>C MANE Select ENSP00000344456.5:n.1683+5G>C
ENST00000396185.8:c.1683+5G>C ENSP00000379488.3:n.1683+5G>C
ENST00000405570.6:c.1683+5G>C ENSP00000385604.1:n.1683+5G>C
ENST00000431914.6:c.1683+5G>C ENSP00000412219.2:n.1683+5G>C
ENST00000433400.6:c.1683+5G>C ENSP00000387455.2:n.1683+5G>C
ENST00000441708.2:c.1683+5G>C ENSP00000401599.2:n.1683+5G>C
ENST00000450969.6:c.1683+5G>C ENSP00000409302.2:n.1683+5G>C
ENST00000453024.6:c.1662+5G>C ENSP00000411226.1:n.1662+5G>C
ENST00000465552.2:n.144+5G>C
ENST00000485265.2:n.894G>C
ENST00000642248.1:c.1683+5G>C ENSP00000495244.1:n.1683+5G>C
ENST00000642315.1:c.1683+5G>C ENSP00000495076.1:n.1683+5G>C
ENST00000642426.1:c.1683+5G>C ENSP00000495719.1:n.1683+5G>C
ENST00000642836.1:c.1662+5G>C ENSP00000496295.1:n.1662+5G>C
ENST00000642886.1:c.1572+5G>C ENSP00000496020.1:n.1572+5G>C
ENST00000642986.1:c.1551+5G>C ENSP00000494422.1:n.1551+5G>C
ENST00000642992.1:c.1683+5G>C ENSP00000496385.1:n.1683+5G>C
ENST00000643031.1:c.1683+5G>C ENSP00000495450.1:n.1683+5G>C
ENST00000643052.1:n.2191G>C
ENST00000643297.1:c.1683+5G>C ENSP00000494677.1:n.1683+5G>C
ENST00000643541.1:c.1683+5G>C ENSP00000494411.1:n.1683+5G>C
ENST00000643865.1:n.2075G>C
ENST00000643977.1:c.1683+5G>C ENSP00000494053.1:n.1683+5G>C
ENST00000643992.1:c.1683+5G>C ENSP00000493610.1:n.1683+5G>C
ENST00000644138.1:c.1683+5G>C ENSP00000496649.1:n.1683+5G>C
ENST00000644395.1:n.445+5G>C
ENST00000644524.1:c.1662+5G>C ENSP00000494780.1:n.1662+5G>C
ENST00000644678.1:c.1662+5G>C ENSP00000495794.1:n.1662+5G>C
ENST00000644867.1:c.1683+5G>C ENSP00000495992.1:n.1683+5G>C
ENST00000644873.1:c.1683+5G>C ENSP00000496511.1:n.1683+5G>C
ENST00000644906.1:c.522+5G>C ENSP00000496584.1:n.522+5G>C
ENST00000645210.1:c.1683+5G>C ENSP00000496180.1:n.1683+5G>C
ENST00000645276.1:c.1689+5G>C ENSP00000494654.1:n.1689+5G>C
ENST00000645305.1:n.2087+5G>C
ENST00000645320.1:c.1683+5G>C ENSP00000495360.1:n.1683+5G>C
ENST00000645493.1:c.1662+5G>C ENSP00000494467.1:n.1662+5G>C
ENST00000645763.1:n.1025G>C
ENST00000645900.1:c.1662+5G>C ENSP00000495286.1:n.1662+5G>C
ENST00000645927.1:c.697+5G>C
ENST00000645982.1:c.1683+5G>C ENSP00000494845.1:n.1683+5G>C
ENST00000646074.1:c.1683+5G>C ENSP00000494263.1:n.1683+5G>C
ENST00000646116.1:c.1662+5G>C ENSP00000495426.1:n.1662+5G>C
ENST00000646174.1:c.1662+5G>C ENSP00000495161.1:n.1662+5G>C
ENST00000646369.1:c.1683+5G>C ENSP00000494914.1:n.1683+5G>C
ENST00000646381.1:c.1662+5G>C ENSP00000496067.1:n.1662+5G>C
ENST00000646725.1:c.1683+5G>C ENSP00000496021.1:n.1683+5G>C
ENST00000647021.1:n.2204+5G>C
ENST00000647264.1:c.1596+5G>C ENSP00000494849.1:n.1596+5G>C
ENST00000647390.1:c.1683+5G>C ENSP00000493533.1:n.1683+5G>C
ENST00000647413.1:c.1683+5G>C ENSP00000493583.1:n.1683+5G>C
ENST00000349496.9:c.1683+5G>C ENSP00000344456.5:n.1683+5G>C
ENST00000396183.7:c.1683+5G>C ENSP00000379486.3:n.1683+5G>C
ENST00000396185.7:c.1683+5G>C ENSP00000379488.3:n.1683+5G>C
ENST00000405570.5:c.1683+5G>C ENSP00000385604.1:n.1683+5G>C
ENST00000453024.5:c.1662+5G>C ENSP00000411226.1:n.1662+5G>C
ENST00000465552.1:n.144+5G>C
NM_001098209.1:c.1683+5G>C NP_001091679.1:n.1683+5G>C
NM_001098210.1:c.1683+5G>C NP_001091680.1:n.1683+5G>C
NM_001904.3:c.1683+5G>C NP_001895.1:n.1683+5G>C
XM_005264886.2:c.1683+5G>C XP_005264943.1:n.1683+5G>C
XM_006712983.1:c.1662+5G>C XP_006713046.1:n.1662+5G>C
XM_006712984.1:c.1662+5G>C XP_006713047.1:n.1662+5G>C
XM_006712985.1:c.1683+5G>C XP_006713048.1:n.1683+5G>C
NM_001330729.1:c.1662+5G>C NP_001317658.1:n.1662+5G>C
XM_006712983.2:c.1662+5G>C XP_006713046.1:n.1662+5G>C
XM_017005738.1:c.1683+5G>C XP_016861227.1:n.1683+5G>C
XM_024453356.1:c.1683+5G>C XP_024309124.1:n.1683+5G>C
XM_024453357.1:c.1683+5G>C XP_024309125.1:n.1683+5G>C
XM_024453358.1:c.1683+5G>C XP_024309126.1:n.1683+5G>C
XM_024453359.1:c.1662+5G>C XP_024309127.1:n.1662+5G>C
XM_024453360.1:c.1662+5G>C XP_024309128.1:n.1662+5G>C
NM_001904.4:c.1683+5G>C MANE Select NP_001895.1:n.1683+5G>C
NM_001098209.2:c.1683+5G>C NP_001091679.1:n.1683+5G>C
NM_001098210.2:c.1683+5G>C NP_001091680.1:n.1683+5G>C
NM_001330729.2:c.1662+5G>C NP_001317658.1:n.1662+5G>C
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