Canonical Allele Identifier: CA1941477432

Gene: HTRA1

Linked Data

• dbSNP Id: rs2097503449

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122507260A>T , CM000672.2:g.122507260A>T	GRCh38
NC_000010.10:g.124266776A>T , CM000672.1:g.124266776A>T	GRCh37
NC_000010.9:g.124256766A>T	NCBI36
NG_011554.1:g.50736A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368984.8:c.973-110A>T MANE Select	ENSP00000357980.3:n.973-110A>T
ENST00000648167.1:c.655-110A>T	ENSP00000498033.1:n.655-110A>T
ENST00000368984.7:c.973-110A>T	ENSP00000357980.3:n.973-110A>T
ENST00000420892.1:c.196-110A>T	ENSP00000412676.1:n.196-110A>T
NM_002775.4:c.973-110A>T	NP_002766.1:n.973-110A>T
NM_002775.5:c.973-110A>T MANE Select	NP_002766.1:n.973-110A>T