Canonical Allele Identifier: CA1941467554
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1591025990

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122472380A>T , CM000672.2:g.122472380A>T GRCh38
NC_000010.10:g.124231896A>T , CM000672.1:g.124231896A>T GRCh37
NC_000010.9:g.124221886A>T NCBI36
NG_011554.1:g.15856A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.472+10256A>T MANE Select ENSP00000357980.3:n.472+10256A>T
ENST00000648167.1:c.154+13671A>T ENSP00000498033.1:n.154+13671A>T
ENST00000368984.7:c.472+10256A>T ENSP00000357980.3:n.472+10256A>T
NM_002775.4:c.472+10256A>T NP_002766.1:n.472+10256A>T
NM_002775.5:c.472+10256A>T MANE Select NP_002766.1:n.472+10256A>T