Canonical Allele Identifier: CA378606229
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs2133905402

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122462001C>T , CM000672.2:g.122462001C>T GRCh38
NC_000010.10:g.124221517C>T , CM000672.1:g.124221517C>T GRCh37
NC_000010.9:g.124211507C>T NCBI36
NG_011554.1:g.5477C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.349C>T MANE Select ENSP00000357980.3:p.Pro117Ser
ENST00000648167.1:c.154+3292C>T ENSP00000498033.1:n.154+3292C>T
ENST00000368984.7:c.349C>T ENSP00000357980.3:p.Pro117Ser
NM_002775.4:c.349C>T NP_002766.1:p.Pro117Ser
NM_002775.5:c.349C>T MANE Select NP_002766.1:p.Pro117Ser