Canonical Allele Identifier: CA367069691
Gene: HOXA13 HGNC NCBI

Linked Data

dbSNP Id: rs2115471178

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198274C>G , CM000669.2:g.27198274C>G GRCh38
NC_000007.13:g.27237893C>G , CM000669.1:g.27237893C>G GRCh37
NC_000007.12:g.27204418C>G NCBI36
NG_008181.1:g.6833G>C
NG_008181.2:g.6833G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000649031.1:c.1091G>C MANE Select ENSP00000497112.1:p.Arg364Pro
ENST00000222753.5:c.1091G>C ENSP00000222753.4:p.Arg364Pro
NM_000522.4:c.1091G>C NP_000513.2:p.Arg364Pro
XM_011515344.1:c.1091G>C XP_011513646.1:p.Arg364Pro
NM_000522.5:c.1091G>C MANE Select NP_000513.2:p.Arg364Pro