Canonical Allele Identifier: CA349353486
Gene: HOXD13 HGNC NCBI

Linked Data

ClinVar Variation Id: 2818313
ClinVar RCV Id: RCV003713654

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176093671G>A , CM000664.2:g.176093671G>A GRCh38
NC_000002.11:g.176958399G>A , CM000664.1:g.176958399G>A GRCh37
NC_000002.10:g.176666645G>A NCBI36
NG_008137.1:g.5868G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000392539.4:c.781G>A MANE Select ENSP00000376322.3:p.Gly261Arg
ENST00000392539.3:c.781G>A ENSP00000376322.3:p.Gly261Arg
NM_000523.3:c.781G>A NP_000514.2:p.Gly261Arg
XM_011511068.1:c.725-809G>A XP_011509370.1:n.725-809G>A
XM_011511068.2:c.725-809G>A XP_011509370.1:n.725-809G>A
NM_000523.4:c.781G>A MANE Select NP_000514.2:p.Gly261Arg