Canonical Allele Identifier: CA2270891810

Gene: AXIN2

Linked Data

• dbSNP Id: rs2044221121

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.65553386A>G , CM000679.2:g.65553386A>G	GRCh38
NC_000017.10:g.63549504A>G , CM000679.1:g.63549504A>G	GRCh37
NC_000017.9:g.60979966A>G	NCBI36
NG_012142.1:g.13237T>C , LRG_296:g.13237T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000307078.10:c.816-3726T>C MANE Select	ENSP00000302625.5:n.816-3726T>C
ENST00000307078.9:c.816-3726T>C	ENSP00000302625.5:n.816-3726T>C
ENST00000375702.5:c.816-3726T>C	ENSP00000364854.5:n.816-3726T>C
ENST00000577662.1:c.1131-3726T>C
ENST00000611991.1:c.396+4839T>C	ENSP00000481191.1:n.396+4839T>C
ENST00000618960.4:c.816-3726T>C	ENSP00000478916.1:n.816-3726T>C
NM_004655.3:c.816-3726T>C , LRG_296t1:c.816-3726T>C	NP_004646.3:n.816-3726T>C
XM_011525319.1:c.816-3726T>C	XP_011523621.1:n.816-3726T>C
XM_011525320.1:c.816-3726T>C	XP_011523622.1:n.816-3726T>C
XM_011525321.1:c.816-3726T>C	XP_011523623.1:n.816-3726T>C
XM_011525322.1:c.816-3726T>C	XP_011523624.1:n.816-3726T>C
NM_001363813.1:c.816-3726T>C	NP_001350742.1:n.816-3726T>C
NM_004655.4:c.816-3726T>C MANE Select	NP_004646.3:n.816-3726T>C
XM_011525319.2:c.816-3726T>C	XP_011523621.1:n.816-3726T>C
XM_011525321.2:c.816-3726T>C	XP_011523623.1:n.816-3726T>C
XM_017025192.1:c.816-3726T>C	XP_016880681.1:n.816-3726T>C
XM_017025193.1:c.816-3726T>C	XP_016880682.1:n.816-3726T>C