Canonical Allele Identifier: CA2611246678
Gene: HTRA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506955G>A , CM000672.2:g.122506955G>A GRCh38
NC_000010.10:g.124266471G>A , CM000672.1:g.124266471G>A GRCh37
NC_000010.9:g.124256461G>A NCBI36
NG_011554.1:g.50431G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.972+70G>A MANE Select ENSP00000357980.3:n.972+70G>A
ENST00000648167.1:c.654+70G>A ENSP00000498033.1:n.654+70G>A
ENST00000368984.7:c.972+70G>A ENSP00000357980.3:n.972+70G>A
ENST00000420892.1:c.195+70G>A ENSP00000412676.1:n.195+70G>A
NM_002775.4:c.972+70G>A NP_002766.1:n.972+70G>A
NM_002775.5:c.972+70G>A MANE Select NP_002766.1:n.972+70G>A