Canonical Allele Identifier: CA354076417

Gene: HGD

Linked Data

• MyVariant Identifiers: chr3:g.120365131G>T (hg19) ; chr3:g.120646284G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120646284G>T , CM000665.2:g.120646284G>T	GRCh38
NC_000003.11:g.120365131G>T , CM000665.1:g.120365131G>T	GRCh37
NC_000003.10:g.121847821G>T	NCBI36
NG_011957.1:g.41198C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.632C>A MANE Select	ENSP00000283871.5:p.Pro211His
ENST00000283871.9:c.632C>A	ENSP00000283871.5:p.Pro211His
ENST00000475447.2:c.163C>A
ENST00000492108.5:c.180+689C>A	ENSP00000419838.1:n.180+689C>A
ENST00000494453.1:c.52C>A
NM_000187.3:c.632C>A	NP_000178.2:p.Pro211His
XM_005247412.1:c.549+689C>A	XP_005247469.1:n.549+689C>A
XM_005247413.1:c.632C>A	XP_005247470.1:p.Pro211His
XM_005247414.3:c.632C>A	XP_005247471.1:p.Pro211His
XM_011512746.1:c.632C>A	XP_011511048.1:p.Pro211His
XM_005247412.2:c.549+689C>A	XP_005247469.1:n.549+689C>A
XM_005247413.2:c.632C>A	XP_005247470.1:p.Pro211His
XM_005247414.5:c.632C>A	XP_005247471.1:p.Pro211His
XM_011512746.2:c.632C>A	XP_011511048.1:p.Pro211His
XM_017006277.2:c.209C>A	XP_016861766.1:p.Pro70His
NM_000187.4:c.632C>A MANE Select	NP_000178.2:p.Pro211His