Canonical Allele Identifier: CA1941478266

Gene: HTRA1

Linked Data

• dbSNP Id: rs1565435801

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122509057C>T , CM000672.2:g.122509057C>T	GRCh38
NC_000010.10:g.124268573C>T , CM000672.1:g.124268573C>T	GRCh37
NC_000010.9:g.124258563C>T	NCBI36
NG_011554.1:g.52533C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368984.8:c.1120+287C>T MANE Select	ENSP00000357980.3:n.1120+287C>T
ENST00000648167.1:c.802+287C>T	ENSP00000498033.1:n.802+287C>T
ENST00000368984.7:c.1120+287C>T	ENSP00000357980.3:n.1120+287C>T
ENST00000420892.1:c.343+287C>T	ENSP00000412676.1:n.343+287C>T
NM_002775.4:c.1120+287C>T	NP_002766.1:n.1120+287C>T
NM_002775.5:c.1120+287C>T MANE Select	NP_002766.1:n.1120+287C>T