Canonical Allele Identifier: CA60846706

Gene: HOXD13

Linked Data

• dbSNP Id: rs1022485097
• MyVariant Identifiers: chr2:g.176958410T>A (hg19) ; chr2:g.176093682T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.176093682T>A , CM000664.2:g.176093682T>A	GRCh38
NC_000002.11:g.176958410T>A , CM000664.1:g.176958410T>A	GRCh37
NC_000002.10:g.176666656T>A	NCBI36
NG_008137.1:g.5879T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392539.4:c.781+11T>A MANE Select	ENSP00000376322.3:n.781+11T>A
ENST00000392539.3:c.781+11T>A	ENSP00000376322.3:n.781+11T>A
NM_000523.3:c.781+11T>A	NP_000514.2:n.781+11T>A
XM_011511068.1:c.725-798T>A	XP_011509370.1:n.725-798T>A
XM_011511068.2:c.725-798T>A	XP_011509370.1:n.725-798T>A
NM_000523.4:c.781+11T>A MANE Select	NP_000514.2:n.781+11T>A