Canonical Allele Identifier: CA377979214
Gene: HOGA1 HGNC NCBI

Linked Data

dbSNP Id: rs2041102033
MyVariant Identifiers: chr10:g.99359555A>G (hg19) chr10:g.97599798A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97599798A>G , CM000672.2:g.97599798A>G GRCh38
NC_000010.10:g.99359555A>G , CM000672.1:g.99359555A>G GRCh37
NC_000010.9:g.99349545A>G NCBI36
NG_027922.1:g.20454A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.587A>G MANE Select ENSP00000359680.4:p.Lys196Arg
ENST00000370646.8:c.587A>G ENSP00000359680.4:p.Lys196Arg
ENST00000370647.8:c.212-2059A>G ENSP00000359681.4:n.212-2059A>G
ENST00000370649.3:c.212-2059A>G ENSP00000359683.3:n.212-2059A>G
ENST00000465608.1:n.1431A>G
NM_001134670.1:c.212-2059A>G NP_001128142.1:n.212-2059A>G
NM_138413.3:c.587A>G NP_612422.2:p.Lys196Arg
NM_138413.4:c.587A>G MANE Select NP_612422.2:p.Lys196Arg
NM_001134670.2:c.212-2059A>G NP_001128142.1:n.212-2059A>G
Search 100 bp 5'
Search 100 bp 3'