Canonical Allele Identifier: CA1976650
Gene: HOXD13 HGNC NCBI

Linked Data

dbSNP Id: rs544065459

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176093628G>A , CM000664.2:g.176093628G>A GRCh38
NC_000002.11:g.176958356G>A , CM000664.1:g.176958356G>A GRCh37
NC_000002.10:g.176666602G>A NCBI36
NG_008137.1:g.5825G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000392539.4:c.738G>A MANE Select ENSP00000376322.3:p.Lys246=
ENST00000392539.3:c.738G>A ENSP00000376322.3:p.Lys246=
NM_000523.3:c.738G>A NP_000514.2:p.Lys246=
XM_011511068.1:c.725-852G>A XP_011509370.1:n.725-852G>A
XM_011511068.2:c.725-852G>A XP_011509370.1:n.725-852G>A
NM_000523.4:c.738G>A MANE Select NP_000514.2:p.Lys246=