Canonical Allele Identifier: CA1930505020
Gene: HOGA1 HGNC NCBI

Linked Data

dbSNP Id: rs2041093913

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97598970C>T , CM000672.2:g.97598970C>T GRCh38
NC_000010.10:g.99358727C>T , CM000672.1:g.99358727C>T GRCh37
NC_000010.9:g.99348717C>T NCBI36
NG_027922.1:g.19626C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.340+67C>T MANE Select ENSP00000359680.4:n.340+67C>T
ENST00000370646.8:c.340+67C>T ENSP00000359680.4:n.340+67C>T
ENST00000370647.8:c.212-2887C>T ENSP00000359681.4:n.212-2887C>T
ENST00000370649.3:c.212-2887C>T ENSP00000359683.3:n.212-2887C>T
ENST00000465608.1:n.721+67C>T
NM_001134670.1:c.212-2887C>T NP_001128142.1:n.212-2887C>T
NM_138413.3:c.340+67C>T NP_612422.2:n.340+67C>T
NM_138413.4:c.340+67C>T MANE Select NP_612422.2:n.340+67C>T
NM_001134670.2:c.212-2887C>T NP_001128142.1:n.212-2887C>T