Canonical Allele Identifier: CA298371
Gene: AXIN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182001
dbSNP Id: rs8081536

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.65538333C>T , CM000679.2:g.65538333C>T GRCh38
NC_000017.10:g.63534451C>T , CM000679.1:g.63534451C>T GRCh37
NC_000017.9:g.60964913C>T NCBI36
NG_012142.1:g.28290G>A , LRG_296:g.28290G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000307078.10:c.1070G>A MANE Select ENSP00000302625.5:p.Arg357His
ENST00000307078.9:c.1070G>A ENSP00000302625.5:p.Arg357His
ENST00000375702.5:c.1070G>A ENSP00000364854.5:p.Arg357His
ENST00000577662.1:c.1385G>A
ENST00000611991.1:c.397-9633G>A ENSP00000481191.1:n.397-9633G>A
ENST00000618960.4:c.1070G>A ENSP00000478916.1:p.Arg357His
NM_004655.3:c.1070G>A , LRG_296t1:c.1070G>A NP_004646.3:p.Arg357His
XM_011525319.1:c.1070G>A XP_011523621.1:p.Arg357His
XM_011525320.1:c.1070G>A XP_011523622.1:p.Arg357His
XM_011525321.1:c.1070G>A XP_011523623.1:p.Arg357His
XM_011525322.1:c.1070G>A XP_011523624.1:p.Arg357His
NM_001363813.1:c.1070G>A NP_001350742.1:p.Arg357His
NM_004655.4:c.1070G>A MANE Select NP_004646.3:p.Arg357His
XM_011525319.2:c.1070G>A XP_011523621.1:p.Arg357His
XM_011525321.2:c.1070G>A XP_011523623.1:p.Arg357His
XM_017025192.1:c.1070G>A XP_016880681.1:p.Arg357His
XM_017025193.1:c.1070G>A XP_016880682.1:p.Arg357His