Canonical Allele Identifier: CA596378882
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1377445108

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461175G>A , CM000672.2:g.122461175G>A GRCh38
NC_000010.10:g.124220691G>A , CM000672.1:g.124220691G>A GRCh37
NC_000010.9:g.124210681G>A NCBI36
NG_011554.1:g.4651G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000648167.1:c.154+2466G>A ENSP00000498033.1:n.154+2466G>A
XR_946382.1:n.184C>T
XR_946383.1:n.184C>T
XR_946384.1:n.184C>T
XR_946385.1:n.184C>T
XR_946382.2:n.212C>T
XR_946383.2:n.212C>T
XR_946384.2:n.188C>T
XR_946385.2:n.212C>T