Canonical Allele Identifier: CA203972
Gene: HOGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 204281
dbSNP Id: rs796052089

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97598871A>T , CM000672.2:g.97598871A>T GRCh38
NC_000010.10:g.99358628A>T , CM000672.1:g.99358628A>T GRCh37
NC_000010.9:g.99348618A>T NCBI36
NG_027922.1:g.19527A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.308A>T MANE Select ENSP00000359680.4:p.Asn103Ile
ENST00000370646.8:c.308A>T ENSP00000359680.4:p.Asn103Ile
ENST00000370647.8:c.212-2986A>T ENSP00000359681.4:n.212-2986A>T
ENST00000370649.3:c.212-2986A>T ENSP00000359683.3:n.212-2986A>T
ENST00000465608.1:n.689A>T
NM_001134670.1:c.212-2986A>T NP_001128142.1:n.212-2986A>T
NM_138413.3:c.308A>T NP_612422.2:p.Asn103Ile
NM_138413.4:c.308A>T MANE Select NP_612422.2:p.Asn103Ile
NM_001134670.2:c.212-2986A>T NP_001128142.1:n.212-2986A>T