Canonical Allele Identifier: CA435228434

Gene: HGD

Linked Data

• gnomAD v4: 3-120650860-C-T
• MyVariant Identifiers: chr3:g.120369707C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120650860C>T , CM000665.2:g.120650860C>T	GRCh38
NC_000003.11:g.120369707C>T , CM000665.1:g.120369707C>T	GRCh37
NC_000003.10:g.121852397C>T	NCBI36
NG_011957.1:g.36622G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.348G>A MANE Select	ENSP00000283871.5:p.Leu116=
ENST00000283871.9:c.348G>A	ENSP00000283871.5:p.Leu116=
ENST00000476082.2:c.225G>A	ENSP00000419560.2:p.Leu75=
ENST00000485313.5:n.456G>A
NM_000187.3:c.348G>A	NP_000178.2:p.Leu116=
XM_005247412.1:c.348G>A	XP_005247469.1:p.Leu116=
XM_005247413.1:c.348G>A	XP_005247470.1:p.Leu116=
XM_005247414.3:c.348G>A	XP_005247471.1:p.Leu116=
XM_011512746.1:c.348G>A	XP_011511048.1:p.Leu116=
XM_005247412.2:c.348G>A	XP_005247469.1:p.Leu116=
XM_005247413.2:c.348G>A	XP_005247470.1:p.Leu116=
XM_005247414.5:c.348G>A	XP_005247471.1:p.Leu116=
XM_011512746.2:c.348G>A	XP_011511048.1:p.Leu116=
XM_017006277.2:c.-76G>A	XP_016861766.1:n.-76G>A
NM_000187.4:c.348G>A MANE Select	NP_000178.2:p.Leu116=