Canonical Allele Identifier: CA350946
Gene: HTRA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 221231
ClinVar RCV Id: RCV000206946
dbSNP Id: rs864622783

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122507369G>A , CM000672.2:g.122507369G>A GRCh38
NC_000010.10:g.124266885G>A , CM000672.1:g.124266885G>A GRCh37
NC_000010.9:g.124256875G>A NCBI36
NG_011554.1:g.50845G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.973-1G>A MANE Select ENSP00000357980.3:n.973-1G>A
ENST00000648167.1:c.655-1G>A ENSP00000498033.1:n.655-1G>A
ENST00000368984.7:c.973-1G>A ENSP00000357980.3:n.973-1G>A
ENST00000420892.1:c.196-1G>A ENSP00000412676.1:n.196-1G>A
NM_002775.4:c.973-1G>A NP_002766.1:n.973-1G>A
NM_002775.5:c.973-1G>A MANE Select NP_002766.1:n.973-1G>A