Canonical Allele Identifier: CA596578956
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1183326240

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461562C>G , CM000672.2:g.122461562C>G GRCh38
NC_000010.10:g.124221078C>G , CM000672.1:g.124221078C>G GRCh37
NC_000010.9:g.124211068C>G NCBI36
NG_011554.1:g.5038C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.-91C>G MANE Select ENSP00000357980.3:n.-91C>G
ENST00000648167.1:c.154+2853C>G ENSP00000498033.1:n.154+2853C>G
ENST00000368984.7:c.-91C>G ENSP00000357980.3:n.-91C>G
NM_002775.4:c.-91C>G NP_002766.1:n.-91C>G
NM_002775.5:c.-91C>G MANE Select NP_002766.1:n.-91C>G