Canonical Allele Identifier: CA81811071

Gene: HGD

Linked Data

• dbSNP Id: rs938556638
• gnomAD v4: 3-120675765-T-C
• MyVariant Identifiers: chr3:g.120394612T>C (hg19) ; chr3:g.120675765T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120675765T>C , CM000665.2:g.120675765T>C	GRCh38
NC_000003.11:g.120394612T>C , CM000665.1:g.120394612T>C	GRCh37
NC_000003.10:g.121877302T>C	NCBI36
NG_011957.1:g.11717A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.87+27A>G MANE Select	ENSP00000283871.5:n.87+27A>G
ENST00000283871.9:c.87+27A>G	ENSP00000283871.5:n.87+27A>G
ENST00000466528.5:n.113+27A>G
ENST00000476082.2:c.53+27A>G	ENSP00000419560.2:n.53+27A>G
ENST00000480862.1:n.245+27A>G
ENST00000485313.5:n.195+27A>G
ENST00000488183.5:n.345+27A>G
NM_000187.3:c.87+27A>G	NP_000178.2:n.87+27A>G
XM_005247412.1:c.87+27A>G	XP_005247469.1:n.87+27A>G
XM_005247413.1:c.87+27A>G	XP_005247470.1:n.87+27A>G
XM_005247414.3:c.87+27A>G	XP_005247471.1:n.87+27A>G
XM_011512746.1:c.87+27A>G	XP_011511048.1:n.87+27A>G
XM_005247412.2:c.87+27A>G	XP_005247469.1:n.87+27A>G
XM_005247413.2:c.87+27A>G	XP_005247470.1:n.87+27A>G
XM_005247414.5:c.87+27A>G	XP_005247471.1:n.87+27A>G
XM_011512746.2:c.87+27A>G	XP_011511048.1:n.87+27A>G
XM_017006277.2:c.-337+27A>G	XP_016861766.1:n.-337+27A>G
NM_000187.4:c.87+27A>G MANE Select	NP_000178.2:n.87+27A>G