Canonical Allele Identifier: CA1930504967
Gene: HOGA1 HGNC NCBI

Linked Data

dbSNP Id: rs1589907742

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97598926C>G , CM000672.2:g.97598926C>G GRCh38
NC_000010.10:g.99358683C>G , CM000672.1:g.99358683C>G GRCh37
NC_000010.9:g.99348673C>G NCBI36
NG_027922.1:g.19582C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.340+23C>G MANE Select ENSP00000359680.4:n.340+23C>G
ENST00000370646.8:c.340+23C>G ENSP00000359680.4:n.340+23C>G
ENST00000370647.8:c.212-2931C>G ENSP00000359681.4:n.212-2931C>G
ENST00000370649.3:c.212-2931C>G ENSP00000359683.3:n.212-2931C>G
ENST00000465608.1:n.721+23C>G
NM_001134670.1:c.212-2931C>G NP_001128142.1:n.212-2931C>G
NM_138413.3:c.340+23C>G NP_612422.2:n.340+23C>G
NM_138413.4:c.340+23C>G MANE Select NP_612422.2:n.340+23C>G
NM_001134670.2:c.212-2931C>G NP_001128142.1:n.212-2931C>G