Canonical Allele Identifier: CA354076844

Gene: HGD

Linked Data

• MyVariant Identifiers: chr3:g.120365212C>G (hg19) ; chr3:g.120646365C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120646365C>G , CM000665.2:g.120646365C>G	GRCh38
NC_000003.11:g.120365212C>G , CM000665.1:g.120365212C>G	GRCh37
NC_000003.10:g.121847902C>G	NCBI36
NG_011957.1:g.41117G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.551G>C MANE Select	ENSP00000283871.5:p.Arg184Thr
ENST00000283871.9:c.551G>C	ENSP00000283871.5:p.Arg184Thr
ENST00000475447.2:c.82G>C
ENST00000492108.5:c.180+608G>C	ENSP00000419838.1:n.180+608G>C
NM_000187.3:c.551G>C	NP_000178.2:p.Arg184Thr
XM_005247412.1:c.549+608G>C	XP_005247469.1:n.549+608G>C
XM_005247413.1:c.551G>C	XP_005247470.1:p.Arg184Thr
XM_005247414.3:c.551G>C	XP_005247471.1:p.Arg184Thr
XM_011512746.1:c.551G>C	XP_011511048.1:p.Arg184Thr
XM_005247412.2:c.549+608G>C	XP_005247469.1:n.549+608G>C
XM_005247413.2:c.551G>C	XP_005247470.1:p.Arg184Thr
XM_005247414.5:c.551G>C	XP_005247471.1:p.Arg184Thr
XM_011512746.2:c.551G>C	XP_011511048.1:p.Arg184Thr
XM_017006277.2:c.128G>C	XP_016861766.1:p.Arg43Thr
NM_000187.4:c.551G>C MANE Select	NP_000178.2:p.Arg184Thr