Canonical Allele Identifier: CA2722608608
Gene: HOGA1 HGNC NCBI

Linked Data

dbSNP Id: rs2135722374

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97599917T>C , CM000672.2:g.97599917T>C GRCh38
NC_000010.10:g.99359674T>C , CM000672.1:g.99359674T>C GRCh37
NC_000010.9:g.99349664T>C NCBI36
NG_027922.1:g.20573T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.603+103T>C MANE Select ENSP00000359680.4:n.603+103T>C
ENST00000370642.4:c.13+103T>C
ENST00000370646.8:c.603+103T>C ENSP00000359680.4:n.603+103T>C
ENST00000370647.8:c.212-1940T>C ENSP00000359681.4:n.212-1940T>C
ENST00000370649.3:c.212-1940T>C ENSP00000359683.3:n.212-1940T>C
ENST00000465608.1:n.1550T>C
NM_001134670.1:c.212-1940T>C NP_001128142.1:n.212-1940T>C
NM_138413.3:c.603+103T>C NP_612422.2:n.603+103T>C
NM_138413.4:c.603+103T>C MANE Select NP_612422.2:n.603+103T>C
NM_001134670.2:c.212-1940T>C NP_001128142.1:n.212-1940T>C