Canonical Allele Identifier: CA354073732

Gene: HGD

Linked Data

• dbSNP Id: rs120074170
• gnomAD v2: 3-120357409-A-G
• gnomAD v3: 3-120638562-A-G
• gnomAD v4: 3-120638562-A-G
• MyVariant Identifiers: chr3:g.120357409A>G (hg19) ; chr3:g.120638562A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120638562A>G , CM000665.2:g.120638562A>G	GRCh38
NC_000003.11:g.120357409A>G , CM000665.1:g.120357409A>G	GRCh37
NC_000003.10:g.121840099A>G	NCBI36
NG_011957.1:g.48920T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000283871.10:c.899T>C MANE Select	ENSP00000283871.5:p.Val300Ala
ENST00000283871.9:c.899T>C	ENSP00000283871.5:p.Val300Ala
ENST00000470321.1:n.239T>C
ENST00000475447.2:c.307+3027T>C
ENST00000492108.5:c.285+3027T>C	ENSP00000419838.1:n.285+3027T>C
ENST00000494453.1:c.319T>C
NM_000187.3:c.899T>C	NP_000178.2:p.Val300Ala
XM_005247412.1:c.674T>C	XP_005247469.1:p.Val225Ala
XM_005247413.1:c.899T>C	XP_005247470.1:p.Val300Ala
XM_011512746.1:c.879+3027T>C	XP_011511048.1:n.879+3027T>C
XM_005247412.2:c.674T>C	XP_005247469.1:p.Val225Ala
XM_005247413.2:c.899T>C	XP_005247470.1:p.Val300Ala
XM_011512746.2:c.879+3027T>C	XP_011511048.1:n.879+3027T>C
XM_017006277.2:c.476T>C	XP_016861766.1:p.Val159Ala
NM_000187.4:c.899T>C MANE Select	NP_000178.2:p.Val300Ala