Canonical Allele Identifier: CA367069699
Gene: HOXA13 HGNC NCBI

Linked Data

dbSNP Id: rs2115471187

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198277T>A , CM000669.2:g.27198277T>A GRCh38
NC_000007.13:g.27237896T>A , CM000669.1:g.27237896T>A GRCh37
NC_000007.12:g.27204421T>A NCBI36
NG_008181.1:g.6830A>T
NG_008181.2:g.6830A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000649031.1:c.1088A>T MANE Select ENSP00000497112.1:p.Glu363Val
ENST00000222753.5:c.1088A>T ENSP00000222753.4:p.Glu363Val
NM_000522.4:c.1088A>T NP_000513.2:p.Glu363Val
XM_011515344.1:c.1088A>T XP_011513646.1:p.Glu363Val
NM_000522.5:c.1088A>T MANE Select NP_000513.2:p.Glu363Val