Canonical Allele Identifier: CA378586981
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1304753475
gnomAD v3: 10-122508771-G-A
gnomAD v4: 10-122508771-G-A
MyVariant Identifiers: chr10:g.124268287G>A (hg19) chr10:g.122508771G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508771G>A , CM000672.2:g.122508771G>A GRCh38
NC_000010.10:g.124268287G>A , CM000672.1:g.124268287G>A GRCh37
NC_000010.9:g.124258277G>A NCBI36
NG_011554.1:g.52247G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.1120+1G>A MANE Select ENSP00000357980.3:n.1120+1G>A
ENST00000648167.1:c.802+1G>A ENSP00000498033.1:n.802+1G>A
ENST00000368984.7:c.1120+1G>A ENSP00000357980.3:n.1120+1G>A
ENST00000420892.1:c.343+1G>A ENSP00000412676.1:n.343+1G>A
NM_002775.4:c.1120+1G>A NP_002766.1:n.1120+1G>A
NM_002775.5:c.1120+1G>A MANE Select NP_002766.1:n.1120+1G>A
Search 100 bp 5'
Search 100 bp 3'