Canonical Allele Identifier: CA1930506979
Gene: HOGA1 HGNC NCBI

Linked Data

dbSNP Id: rs1338748915

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97600189G>T , CM000672.2:g.97600189G>T GRCh38
NC_000010.10:g.99359946G>T , CM000672.1:g.99359946G>T GRCh37
NC_000010.9:g.99349936G>T NCBI36
NG_027922.1:g.20845G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000370646.9:c.700+26G>T MANE Select ENSP00000359680.4:n.700+26G>T
ENST00000370642.4:c.110+26G>T
ENST00000370646.8:c.700+26G>T ENSP00000359680.4:n.700+26G>T
ENST00000370647.8:c.212-1668G>T ENSP00000359681.4:n.212-1668G>T
ENST00000370649.3:c.212-1668G>T ENSP00000359683.3:n.212-1668G>T
ENST00000465608.1:n.1822G>T
NM_001134670.1:c.212-1668G>T NP_001128142.1:n.212-1668G>T
NM_138413.3:c.700+26G>T NP_612422.2:n.700+26G>T
NM_138413.4:c.700+26G>T MANE Select NP_612422.2:n.700+26G>T
NM_001134670.2:c.212-1668G>T NP_001128142.1:n.212-1668G>T