Canonical Allele Identifier: CA16606751
Gene: TCF12 HGNC NCBI

Linked Data

ClinVar Variation Id: 392481
ClinVar RCV Id: RCV000419466
dbSNP Id: rs1057524509
MyVariant Identifiers: chr15:g.57535669G>T (hg19) chr15:g.57243471G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.57243471G>T , CM000677.2:g.57243471G>T GRCh38
NC_000015.9:g.57535669G>T , CM000677.1:g.57535669G>T GRCh37
NC_000015.8:g.55322961G>T NCBI36
NG_033851.1:g.329837G>T
NG_033851.2:g.330382G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000333725.10:c.1036-1G>T MANE Select ENSP00000331057.6:n.1036-1G>T
ENST00000267811.9:c.1036-1G>T ENSP00000267811.5:n.1036-1G>T
ENST00000333725.9:c.1036-1G>T ENSP00000331057.5:n.1036-1G>T
ENST00000343827.7:c.526-1G>T ENSP00000342459.3:n.526-1G>T
ENST00000438423.6:c.1036-1G>T ENSP00000388940.2:n.1036-1G>T
ENST00000537840.5:c.328-1G>T ENSP00000444696.1:n.328-1G>T
ENST00000543579.5:c.526-1G>T ENSP00000440017.1:n.526-1G>T
ENST00000557843.5:c.1036-1G>T ENSP00000453737.1:n.1036-1G>T
ENST00000559609.5:c.1024-1G>T ENSP00000453876.1:n.1024-1G>T
ENST00000560190.5:n.403-29559G>T
ENST00000560764.5:n.871-1G>T
ENST00000561235.5:n.775-1G>T
ENST00000561346.5:n.771-1G>T
NM_001306219.1:c.526-1G>T NP_001293148.1:n.526-1G>T
NM_001306220.1:c.328-1G>T NP_001293149.1:n.328-1G>T
NM_003205.3:c.1036-1G>T NP_003196.1:n.1036-1G>T
NM_207036.1:c.1036-1G>T NP_996919.1:n.1036-1G>T
NM_207037.1:c.1036-1G>T NP_996920.1:n.1036-1G>T
NM_207038.1:c.1036-1G>T NP_996921.1:n.1036-1G>T
NM_207040.1:c.526-1G>T NP_996923.1:n.526-1G>T
XM_005254613.3:c.862-1G>T XP_005254670.1:n.862-1G>T
XM_011521959.1:c.1072-1G>T XP_011520261.1:n.1072-1G>T
XM_011521960.1:c.1072-1G>T XP_011520262.1:n.1072-1G>T
XM_011521961.1:c.1072-1G>T XP_011520263.1:n.1072-1G>T
XM_011521962.1:c.1072-1G>T XP_011520264.1:n.1072-1G>T
XM_011521963.1:c.1072-1G>T XP_011520265.1:n.1072-1G>T
XM_011521965.1:c.388-1G>T XP_011520267.1:n.388-1G>T
XM_011521966.1:c.328-1G>T XP_011520268.1:n.328-1G>T
XM_011521967.1:c.388-1G>T XP_011520269.1:n.388-1G>T
XM_011521969.1:c.526-1G>T XP_011520271.1:n.526-1G>T
NM_001306219.2:c.526-1G>T NP_001293148.1:n.526-1G>T
NM_001306220.2:c.328-1G>T NP_001293149.1:n.328-1G>T
NM_001322151.1:c.1036-1G>T NP_001309080.1:n.1036-1G>T
NM_001322152.1:c.1036-1G>T NP_001309081.1:n.1036-1G>T
NM_001322154.1:c.379-1G>T NP_001309083.1:n.379-1G>T
NM_001322156.1:c.862-1G>T NP_001309085.1:n.862-1G>T
NM_001322157.1:c.1036-1G>T NP_001309086.1:n.1036-1G>T
NM_001322158.1:c.862-1G>T NP_001309087.1:n.862-1G>T
NM_001322159.1:c.1036-1G>T NP_001309088.1:n.1036-1G>T
NM_001322161.1:c.1036-1G>T NP_001309090.1:n.1036-1G>T
NM_001322162.1:c.1036-1G>T NP_001309091.1:n.1036-1G>T
NM_001322164.1:c.1072-1G>T NP_001309093.1:n.1072-1G>T
NM_001322165.1:c.1036-1G>T NP_001309094.1:n.1036-1G>T
XM_011521959.3:c.1072-1G>T XP_011520261.1:n.1072-1G>T
XM_011521960.3:c.1072-1G>T XP_011520262.1:n.1072-1G>T
XM_011521961.3:c.1072-1G>T XP_011520263.1:n.1072-1G>T
XM_011521962.3:c.1072-1G>T XP_011520264.1:n.1072-1G>T
XM_011521963.3:c.1072-1G>T XP_011520265.1:n.1072-1G>T
XM_011521965.2:c.388-1G>T XP_011520267.1:n.388-1G>T
XM_011521966.2:c.328-1G>T XP_011520268.1:n.328-1G>T
XM_011521967.2:c.388-1G>T XP_011520269.1:n.388-1G>T
XM_017022520.2:c.1036-1G>T XP_016878009.1:n.1036-1G>T
NM_001306219.3:c.526-1G>T NP_001293148.1:n.526-1G>T
NM_001306220.3:c.328-1G>T NP_001293149.1:n.328-1G>T
NM_001322152.2:c.1036-1G>T NP_001309081.1:n.1036-1G>T
NM_001322154.2:c.379-1G>T NP_001309083.1:n.379-1G>T
NM_001322156.2:c.862-1G>T NP_001309085.1:n.862-1G>T
NM_001322157.2:c.1036-1G>T NP_001309086.1:n.1036-1G>T
NM_001322158.2:c.862-1G>T NP_001309087.1:n.862-1G>T
NM_001322159.2:c.1036-1G>T NP_001309088.1:n.1036-1G>T
NM_001322161.2:c.1036-1G>T NP_001309090.1:n.1036-1G>T
NM_001322162.2:c.1036-1G>T NP_001309091.1:n.1036-1G>T
NM_001322164.2:c.1072-1G>T NP_001309093.1:n.1072-1G>T
NM_001322165.2:c.1036-1G>T NP_001309094.1:n.1036-1G>T
NM_003205.4:c.1036-1G>T NP_003196.1:n.1036-1G>T
NM_207036.2:c.1036-1G>T NP_996919.1:n.1036-1G>T
NM_207037.2:c.1036-1G>T MANE Select NP_996920.1:n.1036-1G>T
NM_207038.2:c.1036-1G>T NP_996921.1:n.1036-1G>T
NM_207040.2:c.526-1G>T NP_996923.1:n.526-1G>T
NM_001322151.2:c.1036-1G>T NP_001309080.1:n.1036-1G>T
NM_001322157.3:c.1036-1G>T NP_001309086.1:n.1036-1G>T
NM_001322159.3:c.1036-1G>T NP_001309088.1:n.1036-1G>T
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