Canonical Allele Identifier: CA349353100

Gene: HOXD13

Linked Data

• MyVariant Identifiers: chr2:g.176958225G>T (hg19) ; chr2:g.176093497G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.176093497G>T , CM000664.2:g.176093497G>T	GRCh38
NC_000002.11:g.176958225G>T , CM000664.1:g.176958225G>T	GRCh37
NC_000002.10:g.176666471G>T	NCBI36
NG_008137.1:g.5694G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392539.4:c.607G>T MANE Select	ENSP00000376322.3:p.Val203Leu
ENST00000392539.3:c.607G>T	ENSP00000376322.3:p.Val203Leu
NM_000523.3:c.607G>T	NP_000514.2:p.Val203Leu
XM_011511068.1:c.725-983G>T	XP_011509370.1:n.725-983G>T
XM_011511068.2:c.725-983G>T	XP_011509370.1:n.725-983G>T
NM_000523.4:c.607G>T MANE Select	NP_000514.2:p.Val203Leu