Canonical Allele Identifier: CA1941459094
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs2097481212

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461569C>T , CM000672.2:g.122461569C>T GRCh38
NC_000010.10:g.124221085C>T , CM000672.1:g.124221085C>T GRCh37
NC_000010.9:g.124211075C>T NCBI36
NG_011554.1:g.5045C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.-84C>T MANE Select ENSP00000357980.3:n.-84C>T
ENST00000648167.1:c.154+2860C>T ENSP00000498033.1:n.154+2860C>T
ENST00000368984.7:c.-84C>T ENSP00000357980.3:n.-84C>T
NM_002775.4:c.-84C>T NP_002766.1:n.-84C>T
NM_002775.5:c.-84C>T MANE Select NP_002766.1:n.-84C>T