Canonical Allele Identifier: CA13166191
Gene: HOGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1234774
ClinVar RCV Id: RCV001621538
dbSNP Id: rs2297644

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97599982T>C , CM000672.2:g.97599982T>C GRCh38
NC_000010.10:g.99359739T>C , CM000672.1:g.99359739T>C GRCh37
NC_000010.9:g.99349729T>C NCBI36
NG_027922.1:g.20638T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370646.9:c.604-85T>C MANE Select ENSP00000359680.4:n.604-85T>C
ENST00000370642.4:c.14-85T>C
ENST00000370646.8:c.604-85T>C ENSP00000359680.4:n.604-85T>C
ENST00000370647.8:c.212-1875T>C ENSP00000359681.4:n.212-1875T>C
ENST00000370649.3:c.212-1875T>C ENSP00000359683.3:n.212-1875T>C
ENST00000465608.1:n.1615T>C
NM_001134670.1:c.212-1875T>C NP_001128142.1:n.212-1875T>C
NM_138413.3:c.604-85T>C NP_612422.2:n.604-85T>C
NM_138413.4:c.604-85T>C MANE Select NP_612422.2:n.604-85T>C
NM_001134670.2:c.212-1875T>C NP_001128142.1:n.212-1875T>C