Canonical Allele Identifier: CA2667171725

Gene: HGD

Linked Data

• gnomAD v4: 3-120646415-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120646415G>C , CM000665.2:g.120646415G>C	GRCh38
NC_000003.11:g.120365262G>C , CM000665.1:g.120365262G>C	GRCh37
NC_000003.10:g.121847952G>C	NCBI36
NG_011957.1:g.41067C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.550-49C>G MANE Select	ENSP00000283871.5:n.550-49C>G
ENST00000283871.9:c.550-49C>G	ENSP00000283871.5:n.550-49C>G
ENST00000475447.2:c.81-49C>G
ENST00000492108.5:c.180+558C>G	ENSP00000419838.1:n.180+558C>G
NM_000187.3:c.550-49C>G	NP_000178.2:n.550-49C>G
XM_005247412.1:c.549+558C>G	XP_005247469.1:n.549+558C>G
XM_005247413.1:c.550-49C>G	XP_005247470.1:n.550-49C>G
XM_005247414.3:c.550-49C>G	XP_005247471.1:n.550-49C>G
XM_011512746.1:c.550-49C>G	XP_011511048.1:n.550-49C>G
XM_005247412.2:c.549+558C>G	XP_005247469.1:n.549+558C>G
XM_005247413.2:c.550-49C>G	XP_005247470.1:n.550-49C>G
XM_005247414.5:c.550-49C>G	XP_005247471.1:n.550-49C>G
XM_011512746.2:c.550-49C>G	XP_011511048.1:n.550-49C>G
XM_017006277.2:c.127-49C>G	XP_016861766.1:n.127-49C>G
NM_000187.4:c.550-49C>G MANE Select	NP_000178.2:n.550-49C>G