Canonical Allele Identifier: CA400676302
Gene: AXIN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1782929
dbSNP Id: rs730881405

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.65536527G>C , CM000679.2:g.65536527G>C GRCh38
NC_000017.10:g.63532645G>C , CM000679.1:g.63532645G>C GRCh37
NC_000017.9:g.60963107G>C NCBI36
NG_012142.1:g.30096C>G , LRG_296:g.30096C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307078.10:c.1934C>G MANE Select ENSP00000302625.5:p.Pro645Arg
ENST00000307078.9:c.1934C>G ENSP00000302625.5:p.Pro645Arg
ENST00000375702.5:c.1739C>G ENSP00000364854.5:p.Pro580Arg
ENST00000578251.1:n.156C>G
ENST00000611991.1:c.397-7827C>G ENSP00000481191.1:n.397-7827C>G
ENST00000618960.4:c.1739C>G ENSP00000478916.1:p.Pro580Arg
NM_004655.3:c.1934C>G , LRG_296t1:c.1934C>G NP_004646.3:p.Pro645Arg
XM_011525319.1:c.1934C>G XP_011523621.1:p.Pro645Arg
XM_011525320.1:c.1934C>G XP_011523622.1:p.Pro645Arg
XM_011525321.1:c.1934C>G XP_011523623.1:p.Pro645Arg
XM_011525322.1:c.1739C>G XP_011523624.1:p.Pro580Arg
NM_001363813.1:c.1739C>G NP_001350742.1:p.Pro580Arg
NM_004655.4:c.1934C>G MANE Select NP_004646.3:p.Pro645Arg
XM_011525319.2:c.1934C>G XP_011523621.1:p.Pro645Arg
XM_011525321.2:c.1934C>G XP_011523623.1:p.Pro645Arg
XM_017025192.1:c.1934C>G XP_016880681.1:p.Pro645Arg
XM_017025193.1:c.1739C>G XP_016880682.1:p.Pro580Arg