Canonical Allele Identifier: CA60846401
Gene: HOXD13 HGNC NCBI

Linked Data

dbSNP Id: rs13392701

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176093433C>A , CM000664.2:g.176093433C>A GRCh38
NC_000002.11:g.176958161C>A , CM000664.1:g.176958161C>A GRCh37
NC_000002.10:g.176666407C>A NCBI36
NG_008137.1:g.5630C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000392539.4:c.543C>A MANE Select ENSP00000376322.3:p.Asn181Lys
ENST00000392539.3:c.543C>A ENSP00000376322.3:p.Asn181Lys
NM_000523.3:c.543C>A NP_000514.2:p.Asn181Lys
XM_011511068.1:c.725-1047C>A XP_011509370.1:n.725-1047C>A
XM_011511068.2:c.725-1047C>A XP_011509370.1:n.725-1047C>A
NM_000523.4:c.543C>A MANE Select NP_000514.2:p.Asn181Lys