Canonical Allele Identifier: CA471092783

Gene: HOGA1

Linked Data

• dbSNP Id: rs764469579
• gnomAD v2: 10-99371341-C-G
• gnomAD v4: 10-97611584-C-G
• MyVariant Identifiers: chr10:g.99371341C>G (hg19) ; chr10:g.97611584C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97611584C>G , CM000672.2:g.97611584C>G	GRCh38
NC_000010.10:g.99371341C>G , CM000672.1:g.99371341C>G	GRCh37
NC_000010.9:g.99361331C>G	NCBI36
NG_027922.1:g.32240C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370646.9:c.909C>G MANE Select	ENSP00000359680.4:p.Arg303=
ENST00000370646.8:c.909C>G	ENSP00000359680.4:p.Arg303=
ENST00000370647.8:c.420C>G	ENSP00000359681.4:p.Arg140=
ENST00000370649.3:c.345+9594C>G	ENSP00000359683.3:n.345+9594C>G
NM_001134670.1:c.420C>G	NP_001128142.1:p.Arg140=
NM_138413.3:c.909C>G	NP_612422.2:p.Arg303=
NM_138413.4:c.909C>G MANE Select	NP_612422.2:p.Arg303=
NM_001134670.2:c.420C>G	NP_001128142.1:p.Arg140=