Canonical Allele Identifier: CA349353131
Gene: HOXD13 HGNC NCBI

Linked Data

dbSNP Id: rs2105379098
MyVariant Identifiers: chr2:g.176958241A>C (hg19) chr2:g.176093513A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176093513A>C , CM000664.2:g.176093513A>C GRCh38
NC_000002.11:g.176958241A>C , CM000664.1:g.176958241A>C GRCh37
NC_000002.10:g.176666487A>C NCBI36
NG_008137.1:g.5710A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000392539.4:c.623A>C MANE Select ENSP00000376322.3:p.Asp208Ala
ENST00000392539.3:c.623A>C ENSP00000376322.3:p.Asp208Ala
NM_000523.3:c.623A>C NP_000514.2:p.Asp208Ala
XM_011511068.1:c.725-967A>C XP_011509370.1:n.725-967A>C
XM_011511068.2:c.725-967A>C XP_011509370.1:n.725-967A>C
NM_000523.4:c.623A>C MANE Select NP_000514.2:p.Asp208Ala
Search 100 bp 5'
Search 100 bp 3'