Canonical Allele Identifier: CA430224529
Gene: HOXD13 HGNC NCBI

Linked Data

dbSNP Id: rs1221715617
MyVariant Identifiers: chr2:g.176958131A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176093403A>T , CM000664.2:g.176093403A>T GRCh38
NC_000002.11:g.176958131A>T , CM000664.1:g.176958131A>T GRCh37
NC_000002.10:g.176666377A>T NCBI36
NG_008137.1:g.5600A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000392539.4:c.513A>T MANE Select ENSP00000376322.3:p.Ser171=
ENST00000392539.3:c.513A>T ENSP00000376322.3:p.Ser171=
NM_000523.3:c.513A>T NP_000514.2:p.Ser171=
XM_011511068.1:c.725-1077A>T XP_011509370.1:n.725-1077A>T
XM_011511068.2:c.725-1077A>T XP_011509370.1:n.725-1077A>T
NM_000523.4:c.513A>T MANE Select NP_000514.2:p.Ser171=
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Search 100 bp 3'