Canonical Allele Identifier: CA349353136
Gene: HOXD13 HGNC NCBI

Linked Data

dbSNP Id: rs749474029

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176093515A>T , CM000664.2:g.176093515A>T GRCh38
NC_000002.11:g.176958243A>T , CM000664.1:g.176958243A>T GRCh37
NC_000002.10:g.176666489A>T NCBI36
NG_008137.1:g.5712A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000392539.4:c.625A>T MANE Select ENSP00000376322.3:p.Met209Leu
ENST00000392539.3:c.625A>T ENSP00000376322.3:p.Met209Leu
NM_000523.3:c.625A>T NP_000514.2:p.Met209Leu
XM_011511068.1:c.725-965A>T XP_011509370.1:n.725-965A>T
XM_011511068.2:c.725-965A>T XP_011509370.1:n.725-965A>T
NM_000523.4:c.625A>T MANE Select NP_000514.2:p.Met209Leu