Canonical Allele Identifier: CA1976641
Gene: HOXD13 HGNC NCBI

Linked Data

dbSNP Id: rs771123279
ExAC: 2:176958260 C / T
gnomAD v2: 2-176958260-C-T
MyVariant Identifiers: chr2:g.176958260C>T (hg19) chr2:g.176093532C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176093532C>T , CM000664.2:g.176093532C>T GRCh38
NC_000002.11:g.176958260C>T , CM000664.1:g.176958260C>T GRCh37
NC_000002.10:g.176666506C>T NCBI36
NG_008137.1:g.5729C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000392539.4:c.642C>T MANE Select ENSP00000376322.3:p.Gly214=
ENST00000392539.3:c.642C>T ENSP00000376322.3:p.Gly214=
NM_000523.3:c.642C>T NP_000514.2:p.Gly214=
XM_011511068.1:c.725-948C>T XP_011509370.1:n.725-948C>T
XM_011511068.2:c.725-948C>T XP_011509370.1:n.725-948C>T
NM_000523.4:c.642C>T MANE Select NP_000514.2:p.Gly214=
Search 100 bp 5'
Search 100 bp 3'