Canonical Allele Identifier: CA203970
Gene: HOGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 204280
dbSNP Id: rs796052088

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97598790G>A , CM000672.2:g.97598790G>A GRCh38
NC_000010.10:g.99358547G>A , CM000672.1:g.99358547G>A GRCh37
NC_000010.9:g.99348537G>A NCBI36
NG_027922.1:g.19446G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.227G>A MANE Select ENSP00000359680.4:p.Gly76Asp
ENST00000370646.8:c.227G>A ENSP00000359680.4:p.Gly76Asp
ENST00000370647.8:c.212-3067G>A ENSP00000359681.4:n.212-3067G>A
ENST00000370649.3:c.212-3067G>A ENSP00000359683.3:n.212-3067G>A
ENST00000465608.1:n.608G>A
NM_001134670.1:c.212-3067G>A NP_001128142.1:n.212-3067G>A
NM_138413.3:c.227G>A NP_612422.2:p.Gly76Asp
NM_138413.4:c.227G>A MANE Select NP_612422.2:p.Gly76Asp
NM_001134670.2:c.212-3067G>A NP_001128142.1:n.212-3067G>A