Canonical Allele Identifier: CA354073282

Gene: HGD

Linked Data

• MyVariant Identifiers: chr3:g.120357305G>A (hg19) ; chr3:g.120638458G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120638458G>A , CM000665.2:g.120638458G>A	GRCh38
NC_000003.11:g.120357305G>A , CM000665.1:g.120357305G>A	GRCh37
NC_000003.10:g.121839995G>A	NCBI36
NG_011957.1:g.49024C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.1003C>T MANE Select	ENSP00000283871.5:p.His335Tyr
ENST00000283871.9:c.1003C>T	ENSP00000283871.5:p.His335Tyr
ENST00000470321.1:n.343C>T
ENST00000475447.2:c.307+3131C>T
ENST00000492108.5:c.285+3131C>T	ENSP00000419838.1:n.285+3131C>T
ENST00000494453.1:c.423C>T
NM_000187.3:c.1003C>T	NP_000178.2:p.His335Tyr
XM_005247412.1:c.778C>T	XP_005247469.1:p.His260Tyr
XM_005247413.1:c.1003C>T	XP_005247470.1:p.His335Tyr
XM_011512746.1:c.879+3131C>T	XP_011511048.1:n.879+3131C>T
XM_005247412.2:c.778C>T	XP_005247469.1:p.His260Tyr
XM_005247413.2:c.1003C>T	XP_005247470.1:p.His335Tyr
XM_011512746.2:c.879+3131C>T	XP_011511048.1:n.879+3131C>T
XM_017006277.2:c.580C>T	XP_016861766.1:p.His194Tyr
NM_000187.4:c.1003C>T MANE Select	NP_000178.2:p.His335Tyr