Canonical Allele Identifier: CA1941459100
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs2097481215

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461573A>C , CM000672.2:g.122461573A>C GRCh38
NC_000010.10:g.124221089A>C , CM000672.1:g.124221089A>C GRCh37
NC_000010.9:g.124211079A>C NCBI36
NG_011554.1:g.5049A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.-80A>C MANE Select ENSP00000357980.3:n.-80A>C
ENST00000648167.1:c.154+2864A>C ENSP00000498033.1:n.154+2864A>C
ENST00000368984.7:c.-80A>C ENSP00000357980.3:n.-80A>C
NM_002775.4:c.-80A>C NP_002766.1:n.-80A>C
NM_002775.5:c.-80A>C MANE Select NP_002766.1:n.-80A>C