Canonical Allele Identifier: CA354072940

Gene: HGD

Linked Data

• MyVariant Identifiers: chr3:g.120352131C>G (hg19) ; chr3:g.120633284C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120633284C>G , CM000665.2:g.120633284C>G	GRCh38
NC_000003.11:g.120352131C>G , CM000665.1:g.120352131C>G	GRCh37
NC_000003.10:g.121834821C>G	NCBI36
NG_011957.1:g.54198G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000283871.10:c.1051G>C MANE Select	ENSP00000283871.5:p.Glu351Gln
ENST00000283871.9:c.1051G>C	ENSP00000283871.5:p.Glu351Gln
ENST00000470321.1:n.391G>C
ENST00000492108.5:c.330G>C	ENSP00000419838.1:n.330G>C
NM_000187.3:c.1051G>C	NP_000178.2:p.Glu351Gln
XM_005247412.1:c.826G>C	XP_005247469.1:p.Glu276Gln
XM_005247412.2:c.826G>C	XP_005247469.1:p.Glu276Gln
XM_017006277.2:c.628G>C	XP_016861766.1:p.Glu210Gln
NM_000187.4:c.1051G>C MANE Select	NP_000178.2:p.Glu351Gln