Canonical Allele Identifier: CA5634056
Gene: HOGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1294832
ClinVar RCV Id: RCV001720736
dbSNP Id: rs74155508
ExAC: 10:99358686 G / C
gnomAD v2: 10-99358686-G-C
gnomAD v3: 10-97598929-G-C
gnomAD v4: 10-97598929-G-C
MyVariant Identifiers: chr10:g.99358686G>C (hg19) chr10:g.97598929G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97598929G>C , CM000672.2:g.97598929G>C GRCh38
NC_000010.10:g.99358686G>C , CM000672.1:g.99358686G>C GRCh37
NC_000010.9:g.99348676G>C NCBI36
NG_027922.1:g.19585G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.340+26G>C MANE Select ENSP00000359680.4:n.340+26G>C
ENST00000370646.8:c.340+26G>C ENSP00000359680.4:n.340+26G>C
ENST00000370647.8:c.212-2928G>C ENSP00000359681.4:n.212-2928G>C
ENST00000370649.3:c.212-2928G>C ENSP00000359683.3:n.212-2928G>C
ENST00000465608.1:n.721+26G>C
NM_001134670.1:c.212-2928G>C NP_001128142.1:n.212-2928G>C
NM_138413.3:c.340+26G>C NP_612422.2:n.340+26G>C
NM_138413.4:c.340+26G>C MANE Select NP_612422.2:n.340+26G>C
NM_001134670.2:c.212-2928G>C NP_001128142.1:n.212-2928G>C
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