Canonical Allele Identifier: CA349351946
Gene: HOXD13 HGNC NCBI

Linked Data

dbSNP Id: rs536639583
gnomAD v3: 2-176092922-G-T
gnomAD v4: 2-176092922-G-T
MyVariant Identifiers: chr2:g.176957650G>T (hg19) chr2:g.176092922G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176092922G>T , CM000664.2:g.176092922G>T GRCh38
NC_000002.11:g.176957650G>T , CM000664.1:g.176957650G>T GRCh37
NC_000002.10:g.176665896G>T NCBI36
NG_008137.1:g.5119G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000392539.4:c.32G>T MANE Select ENSP00000376322.3:p.Gly11Val
ENST00000392539.3:c.32G>T ENSP00000376322.3:p.Gly11Val
NM_000523.3:c.32G>T NP_000514.2:p.Gly11Val
XM_011511068.1:c.725-1558G>T XP_011509370.1:n.725-1558G>T
XM_011511068.2:c.725-1558G>T XP_011509370.1:n.725-1558G>T
NM_000523.4:c.32G>T MANE Select NP_000514.2:p.Gly11Val
Search 100 bp 5'
Search 100 bp 3'