Canonical Allele Identifier: CA378606305
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1332122012

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122462035A>C , CM000672.2:g.122462035A>C GRCh38
NC_000010.10:g.124221551A>C , CM000672.1:g.124221551A>C GRCh37
NC_000010.9:g.124211541A>C NCBI36
NG_011554.1:g.5511A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.383A>C MANE Select ENSP00000357980.3:p.Asn128Thr
ENST00000648167.1:c.154+3326A>C ENSP00000498033.1:n.154+3326A>C
ENST00000368984.7:c.383A>C ENSP00000357980.3:p.Asn128Thr
NM_002775.4:c.383A>C NP_002766.1:p.Asn128Thr
NM_002775.5:c.383A>C MANE Select NP_002766.1:p.Asn128Thr