Canonical Allele Identifier: CA660865161
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs908625280

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461181C>A , CM000672.2:g.122461181C>A GRCh38
NC_000010.10:g.124220697C>A , CM000672.1:g.124220697C>A GRCh37
NC_000010.9:g.124210687C>A NCBI36
NG_011554.1:g.4657C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000648167.1:c.154+2472C>A ENSP00000498033.1:n.154+2472C>A
XR_946382.1:n.178G>T
XR_946383.1:n.178G>T
XR_946384.1:n.178G>T
XR_946385.1:n.178G>T
XR_946382.2:n.206G>T
XR_946383.2:n.206G>T
XR_946384.2:n.182G>T
XR_946385.2:n.206G>T