Canonical Allele Identifier: CA354076310

Gene: HGD

Linked Data

• gnomAD v4: 3-120646267-C-T
• MyVariant Identifiers: chr3:g.120365114C>T (hg19) ; chr3:g.120646267C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120646267C>T , CM000665.2:g.120646267C>T	GRCh38
NC_000003.11:g.120365114C>T , CM000665.1:g.120365114C>T	GRCh37
NC_000003.10:g.121847804C>T	NCBI36
NG_011957.1:g.41215G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000283871.10:c.649G>A MANE Select	ENSP00000283871.5:p.Gly217Arg
ENST00000283871.9:c.649G>A	ENSP00000283871.5:p.Gly217Arg
ENST00000475447.2:c.180G>A
ENST00000492108.5:c.180+706G>A	ENSP00000419838.1:n.180+706G>A
ENST00000494453.1:c.69G>A
NM_000187.3:c.649G>A	NP_000178.2:p.Gly217Arg
XM_005247412.1:c.549+706G>A	XP_005247469.1:n.549+706G>A
XM_005247413.1:c.649G>A	XP_005247470.1:p.Gly217Arg
XM_005247414.3:c.649G>A	XP_005247471.1:p.Asp217Asn
XM_011512746.1:c.649G>A	XP_011511048.1:p.Gly217Arg
XM_005247412.2:c.549+706G>A	XP_005247469.1:n.549+706G>A
XM_005247413.2:c.649G>A	XP_005247470.1:p.Gly217Arg
XM_005247414.5:c.649G>A	XP_005247471.1:p.Asp217Asn
XM_011512746.2:c.649G>A	XP_011511048.1:p.Gly217Arg
XM_017006277.2:c.226G>A	XP_016861766.1:p.Gly76Arg
NM_000187.4:c.649G>A MANE Select	NP_000178.2:p.Gly217Arg