Canonical Allele Identifier: CA471092054
Gene: HOGA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.99359550C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97599793C>G , CM000672.2:g.97599793C>G GRCh38
NC_000010.10:g.99359550C>G , CM000672.1:g.99359550C>G GRCh37
NC_000010.9:g.99349540C>G NCBI36
NG_027922.1:g.20449C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.582C>G MANE Select ENSP00000359680.4:p.Gly194=
ENST00000370646.8:c.582C>G ENSP00000359680.4:p.Gly194=
ENST00000370647.8:c.212-2064C>G ENSP00000359681.4:n.212-2064C>G
ENST00000370649.3:c.212-2064C>G ENSP00000359683.3:n.212-2064C>G
ENST00000465608.1:n.1426C>G
NM_001134670.1:c.212-2064C>G NP_001128142.1:n.212-2064C>G
NM_138413.3:c.582C>G NP_612422.2:p.Gly194=
NM_138413.4:c.582C>G MANE Select NP_612422.2:p.Gly194=
NM_001134670.2:c.212-2064C>G NP_001128142.1:n.212-2064C>G
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