Canonical Allele Identifier: CA5634306
Gene: HOGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2199695
ClinVar RCV Id: RCV002659720 RCV003447335
dbSNP Id: rs761150081
ExAC: 10:99371340 G / A
gnomAD v2: 10-99371340-G-A
gnomAD v3: 10-97611583-G-A
gnomAD v4: 10-97611583-G-A
COSMIC: COSM4714214
MyVariant Identifiers: chr10:g.99371340G>A (hg19) chr10:g.97611583G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97611583G>A , CM000672.2:g.97611583G>A GRCh38
NC_000010.10:g.99371340G>A , CM000672.1:g.99371340G>A GRCh37
NC_000010.9:g.99361330G>A NCBI36
NG_027922.1:g.32239G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370646.9:c.908G>A MANE Select ENSP00000359680.4:p.Arg303His
ENST00000370646.8:c.908G>A ENSP00000359680.4:p.Arg303His
ENST00000370647.8:c.419G>A ENSP00000359681.4:p.Arg140His
ENST00000370649.3:c.345+9593G>A ENSP00000359683.3:n.345+9593G>A
NM_001134670.1:c.419G>A NP_001128142.1:p.Arg140His
NM_138413.3:c.908G>A NP_612422.2:p.Arg303His
NM_138413.4:c.908G>A MANE Select NP_612422.2:p.Arg303His
NM_001134670.2:c.419G>A NP_001128142.1:p.Arg140His
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