Canonical Allele Identifier: CA14384065
Gene: AXIN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1281490
ClinVar RCV Id: RCV001691622
dbSNP Id: rs11867417

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.65541780T>C , CM000679.2:g.65541780T>C GRCh38
NC_000017.10:g.63537898T>C , CM000679.1:g.63537898T>C GRCh37
NC_000017.9:g.60968360T>C NCBI36
NG_012142.1:g.24843A>G , LRG_296:g.24843A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307078.10:c.957-223A>G MANE Select ENSP00000302625.5:n.957-223A>G
ENST00000307078.9:c.957-223A>G ENSP00000302625.5:n.957-223A>G
ENST00000375702.5:c.957-223A>G ENSP00000364854.5:n.957-223A>G
ENST00000577662.1:c.1272-223A>G
ENST00000611991.1:c.397-13080A>G ENSP00000481191.1:n.397-13080A>G
ENST00000618960.4:c.957-223A>G ENSP00000478916.1:n.957-223A>G
NM_004655.3:c.957-223A>G , LRG_296t1:c.957-223A>G NP_004646.3:n.957-223A>G
XM_011525319.1:c.957-223A>G XP_011523621.1:n.957-223A>G
XM_011525320.1:c.957-223A>G XP_011523622.1:n.957-223A>G
XM_011525321.1:c.957-223A>G XP_011523623.1:n.957-223A>G
XM_011525322.1:c.957-223A>G XP_011523624.1:n.957-223A>G
NM_001363813.1:c.957-223A>G NP_001350742.1:n.957-223A>G
NM_004655.4:c.957-223A>G MANE Select NP_004646.3:n.957-223A>G
XM_011525319.2:c.957-223A>G XP_011523621.1:n.957-223A>G
XM_011525321.2:c.957-223A>G XP_011523623.1:n.957-223A>G
XM_017025192.1:c.957-223A>G XP_016880681.1:n.957-223A>G
XM_017025193.1:c.957-223A>G XP_016880682.1:n.957-223A>G