Canonical Allele Identifier: CA897952707

Gene: HGD

Linked Data

• dbSNP Id: rs769800661
• gnomAD v4: 3-120638678-C-T
• MyVariant Identifiers: chr3:g.120357525C>T (hg19) ; chr3:g.120638678C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120638678C>T , CM000665.2:g.120638678C>T	GRCh38
NC_000003.11:g.120357525C>T , CM000665.1:g.120357525C>T	GRCh37
NC_000003.10:g.121840215C>T	NCBI36
NG_011957.1:g.48804G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.880-97G>A MANE Select	ENSP00000283871.5:n.880-97G>A
ENST00000283871.9:c.880-97G>A	ENSP00000283871.5:n.880-97G>A
ENST00000470321.1:n.220-97G>A
ENST00000475447.2:c.307+2911G>A
ENST00000492108.5:c.285+2911G>A	ENSP00000419838.1:n.285+2911G>A
ENST00000494453.1:c.300-97G>A
NM_000187.3:c.880-97G>A	NP_000178.2:n.880-97G>A
XM_005247412.1:c.655-97G>A	XP_005247469.1:n.655-97G>A
XM_005247413.1:c.880-97G>A	XP_005247470.1:n.880-97G>A
XM_011512746.1:c.879+2911G>A	XP_011511048.1:n.879+2911G>A
XM_005247412.2:c.655-97G>A	XP_005247469.1:n.655-97G>A
XM_005247413.2:c.880-97G>A	XP_005247470.1:n.880-97G>A
XM_011512746.2:c.879+2911G>A	XP_011511048.1:n.879+2911G>A
XM_017006277.2:c.457-97G>A	XP_016861766.1:n.457-97G>A
NM_000187.4:c.880-97G>A MANE Select	NP_000178.2:n.880-97G>A