Canonical Allele Identifier: CA596578967
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1318780799

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461604T>A , CM000672.2:g.122461604T>A GRCh38
NC_000010.10:g.124221120T>A , CM000672.1:g.124221120T>A GRCh37
NC_000010.9:g.124211110T>A NCBI36
NG_011554.1:g.5080T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.-49T>A MANE Select ENSP00000357980.3:n.-49T>A
ENST00000648167.1:c.154+2895T>A ENSP00000498033.1:n.154+2895T>A
ENST00000368984.7:c.-49T>A ENSP00000357980.3:n.-49T>A
NM_002775.4:c.-49T>A NP_002766.1:n.-49T>A
NM_002775.5:c.-49T>A MANE Select NP_002766.1:n.-49T>A