Canonical Allele Identifier: CA378586873
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs2097504282

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508746G>C , CM000672.2:g.122508746G>C GRCh38
NC_000010.10:g.124268262G>C , CM000672.1:g.124268262G>C GRCh37
NC_000010.9:g.124258252G>C NCBI36
NG_011554.1:g.52222G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1096G>C MANE Select ENSP00000357980.3:p.Glu366Gln
ENST00000648167.1:c.778G>C ENSP00000498033.1:p.Glu260Gln
ENST00000368984.7:c.1096G>C ENSP00000357980.3:p.Glu366Gln
ENST00000420892.1:c.319G>C ENSP00000412676.1:p.Glu107Gln
NM_002775.4:c.1096G>C NP_002766.1:p.Glu366Gln
NM_002775.5:c.1096G>C MANE Select NP_002766.1:p.Glu366Gln