Canonical Allele Identifier: CA378606267
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs2133905419

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122462018C>A , CM000672.2:g.122462018C>A GRCh38
NC_000010.10:g.124221534C>A , CM000672.1:g.124221534C>A GRCh37
NC_000010.9:g.124211524C>A NCBI36
NG_011554.1:g.5494C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.366C>A MANE Select ENSP00000357980.3:p.Asp122Glu
ENST00000648167.1:c.154+3309C>A ENSP00000498033.1:n.154+3309C>A
ENST00000368984.7:c.366C>A ENSP00000357980.3:p.Asp122Glu
NM_002775.4:c.366C>A NP_002766.1:p.Asp122Glu
NM_002775.5:c.366C>A MANE Select NP_002766.1:p.Asp122Glu