Canonical Allele Identifier: CA378606406
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs779980320

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122462082C>G , CM000672.2:g.122462082C>G GRCh38
NC_000010.10:g.124221598C>G , CM000672.1:g.124221598C>G GRCh37
NC_000010.9:g.124211588C>G NCBI36
NG_011554.1:g.5558C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.430C>G MANE Select ENSP00000357980.3:p.Arg144Gly
ENST00000648167.1:c.154+3373C>G ENSP00000498033.1:n.154+3373C>G
ENST00000368984.7:c.430C>G ENSP00000357980.3:p.Arg144Gly
NM_002775.4:c.430C>G NP_002766.1:p.Arg144Gly
NM_002775.5:c.430C>G MANE Select NP_002766.1:p.Arg144Gly