Canonical Allele Identifier: CA471092062
Gene: HOGA1 HGNC NCBI

Linked Data

dbSNP Id: rs1589908425
MyVariant Identifiers: chr10:g.99359568T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97599811T>G , CM000672.2:g.97599811T>G GRCh38
NC_000010.10:g.99359568T>G , CM000672.1:g.99359568T>G GRCh37
NC_000010.9:g.99349558T>G NCBI36
NG_027922.1:g.20467T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.600T>G MANE Select ENSP00000359680.4:p.Gly200=
ENST00000370642.4:c.10T>G
ENST00000370646.8:c.600T>G ENSP00000359680.4:p.Gly200=
ENST00000370647.8:c.212-2046T>G ENSP00000359681.4:n.212-2046T>G
ENST00000370649.3:c.212-2046T>G ENSP00000359683.3:n.212-2046T>G
ENST00000465608.1:n.1444T>G
NM_001134670.1:c.212-2046T>G NP_001128142.1:n.212-2046T>G
NM_138413.3:c.600T>G NP_612422.2:p.Gly200=
NM_138413.4:c.600T>G MANE Select NP_612422.2:p.Gly200=
NM_001134670.2:c.212-2046T>G NP_001128142.1:n.212-2046T>G
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