Canonical Allele Identifier: CA349353114
Gene: HOXD13 HGNC NCBI

Linked Data

dbSNP Id: rs2105379080

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176093506T>A , CM000664.2:g.176093506T>A GRCh38
NC_000002.11:g.176958234T>A , CM000664.1:g.176958234T>A GRCh37
NC_000002.10:g.176666480T>A NCBI36
NG_008137.1:g.5703T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000392539.4:c.616T>A MANE Select ENSP00000376322.3:p.Tyr206Asn
ENST00000392539.3:c.616T>A ENSP00000376322.3:p.Tyr206Asn
NM_000523.3:c.616T>A NP_000514.2:p.Tyr206Asn
XM_011511068.1:c.725-974T>A XP_011509370.1:n.725-974T>A
XM_011511068.2:c.725-974T>A XP_011509370.1:n.725-974T>A
NM_000523.4:c.616T>A MANE Select NP_000514.2:p.Tyr206Asn