Canonical Allele Identifier: CA349353278
Gene: HOXD13 HGNC NCBI

Linked Data

dbSNP Id: rs1689365697

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176093579A>G , CM000664.2:g.176093579A>G GRCh38
NC_000002.11:g.176958307A>G , CM000664.1:g.176958307A>G GRCh37
NC_000002.10:g.176666553A>G NCBI36
NG_008137.1:g.5776A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000392539.4:c.689A>G MANE Select ENSP00000376322.3:p.Gln230Arg
ENST00000392539.3:c.689A>G ENSP00000376322.3:p.Gln230Arg
NM_000523.3:c.689A>G NP_000514.2:p.Gln230Arg
XM_011511068.1:c.725-901A>G XP_011509370.1:n.725-901A>G
XM_011511068.2:c.725-901A>G XP_011509370.1:n.725-901A>G
NM_000523.4:c.689A>G MANE Select NP_000514.2:p.Gln230Arg