Canonical Allele Identifier: CA435227860

Gene: HGD

Linked Data

• MyVariant Identifiers: chr3:g.120365121T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120646274T>G , CM000665.2:g.120646274T>G	GRCh38
NC_000003.11:g.120365121T>G , CM000665.1:g.120365121T>G	GRCh37
NC_000003.10:g.121847811T>G	NCBI36
NG_011957.1:g.41208A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000283871.10:c.642A>C MANE Select	ENSP00000283871.5:p.Gly214=
ENST00000283871.9:c.642A>C	ENSP00000283871.5:p.Gly214=
ENST00000475447.2:c.173A>C
ENST00000492108.5:c.180+699A>C	ENSP00000419838.1:n.180+699A>C
ENST00000494453.1:c.62A>C
NM_000187.3:c.642A>C	NP_000178.2:p.Gly214=
XM_005247412.1:c.549+699A>C	XP_005247469.1:n.549+699A>C
XM_005247413.1:c.642A>C	XP_005247470.1:p.Gly214=
XM_005247414.3:c.642A>C	XP_005247471.1:p.Gly214=
XM_011512746.1:c.642A>C	XP_011511048.1:p.Gly214=
XM_005247412.2:c.549+699A>C	XP_005247469.1:n.549+699A>C
XM_005247413.2:c.642A>C	XP_005247470.1:p.Gly214=
XM_005247414.5:c.642A>C	XP_005247471.1:p.Gly214=
XM_011512746.2:c.642A>C	XP_011511048.1:p.Gly214=
XM_017006277.2:c.219A>C	XP_016861766.1:p.Gly73=
NM_000187.4:c.642A>C MANE Select	NP_000178.2:p.Gly214=