Canonical Allele Identifier: CA81786406

Gene: HGD

Linked Data

• dbSNP Id: rs1051076506
• gnomAD v2: 3-120364757-A-G
• gnomAD v3: 3-120645910-A-G
• gnomAD v4: 3-120645910-A-G
• MyVariant Identifiers: chr3:g.120364757A>G (hg19) ; chr3:g.120645910A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120645910A>G , CM000665.2:g.120645910A>G	GRCh38
NC_000003.11:g.120364757A>G , CM000665.1:g.120364757A>G	GRCh37
NC_000003.10:g.121847447A>G	NCBI36
NG_011957.1:g.41572T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.649+357T>C MANE Select	ENSP00000283871.5:n.649+357T>C
ENST00000283871.9:c.649+357T>C	ENSP00000283871.5:n.649+357T>C
ENST00000475447.2:c.180+357T>C
ENST00000492108.5:c.180+1063T>C	ENSP00000419838.1:n.180+1063T>C
ENST00000494453.1:c.69+357T>C
NM_000187.3:c.649+357T>C	NP_000178.2:n.649+357T>C
XM_005247412.1:c.549+1063T>C	XP_005247469.1:n.549+1063T>C
XM_005247413.1:c.649+357T>C	XP_005247470.1:n.649+357T>C
XM_005247414.3:c.649+357T>C	XP_005247471.1:n.649+357T>C
XM_011512746.1:c.649+357T>C	XP_011511048.1:n.649+357T>C
XM_005247412.2:c.549+1063T>C	XP_005247469.1:n.549+1063T>C
XM_005247413.2:c.649+357T>C	XP_005247470.1:n.649+357T>C
XM_005247414.5:c.649+357T>C	XP_005247471.1:n.649+357T>C
XM_011512746.2:c.649+357T>C	XP_011511048.1:n.649+357T>C
XM_017006277.2:c.226+357T>C	XP_016861766.1:n.226+357T>C
NM_000187.4:c.649+357T>C MANE Select	NP_000178.2:n.649+357T>C