Canonical Allele Identifier: CA367069693
Gene: HOXA13 HGNC NCBI

Linked Data

dbSNP Id: rs1784029885

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198275G>A , CM000669.2:g.27198275G>A GRCh38
NC_000007.13:g.27237894G>A , CM000669.1:g.27237894G>A GRCh37
NC_000007.12:g.27204419G>A NCBI36
NG_008181.1:g.6832C>T
NG_008181.2:g.6832C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000649031.1:c.1090C>T MANE Select ENSP00000497112.1:p.Arg364Trp
ENST00000222753.5:c.1090C>T ENSP00000222753.4:p.Arg364Trp
NM_000522.4:c.1090C>T NP_000513.2:p.Arg364Trp
XM_011515344.1:c.1090C>T XP_011513646.1:p.Arg364Trp
NM_000522.5:c.1090C>T MANE Select NP_000513.2:p.Arg364Trp