Canonical Allele Identifier: CA897931470

Gene: HGD

Linked Data

• dbSNP Id: rs1184237766
• MyVariant Identifiers: chr3:g.120389400G>A (hg19) ; chr3:g.120670553G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120670553G>A , CM000665.2:g.120670553G>A	GRCh38
NC_000003.11:g.120389400G>A , CM000665.1:g.120389400G>A	GRCh37
NC_000003.10:g.121872090G>A	NCBI36
NG_011957.1:g.16929C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000283871.10:c.177-21C>T MANE Select	ENSP00000283871.5:n.177-21C>T
ENST00000283871.9:c.177-21C>T	ENSP00000283871.5:n.177-21C>T
ENST00000466528.5:n.203-21C>T
ENST00000476082.2:c.54-21C>T	ENSP00000419560.2:n.54-21C>T
ENST00000485313.5:n.285-21C>T
ENST00000488183.5:n.435-21C>T
NM_000187.3:c.177-21C>T	NP_000178.2:n.177-21C>T
XM_005247412.1:c.177-21C>T	XP_005247469.1:n.177-21C>T
XM_005247413.1:c.177-21C>T	XP_005247470.1:n.177-21C>T
XM_005247414.3:c.177-21C>T	XP_005247471.1:n.177-21C>T
XM_011512746.1:c.177-21C>T	XP_011511048.1:n.177-21C>T
XM_005247412.2:c.177-21C>T	XP_005247469.1:n.177-21C>T
XM_005247413.2:c.177-21C>T	XP_005247470.1:n.177-21C>T
XM_005247414.5:c.177-21C>T	XP_005247471.1:n.177-21C>T
XM_011512746.2:c.177-21C>T	XP_011511048.1:n.177-21C>T
XM_017006277.2:c.-247-21C>T	XP_016861766.1:n.-247-21C>T
NM_000187.4:c.177-21C>T MANE Select	NP_000178.2:n.177-21C>T