Canonical Allele Identifier: CA378586983
Gene: HTRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.124268287G>C (hg19) chr10:g.122508771G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508771G>C , CM000672.2:g.122508771G>C GRCh38
NC_000010.10:g.124268287G>C , CM000672.1:g.124268287G>C GRCh37
NC_000010.9:g.124258277G>C NCBI36
NG_011554.1:g.52247G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.1120+1G>C MANE Select ENSP00000357980.3:n.1120+1G>C
ENST00000648167.1:c.802+1G>C ENSP00000498033.1:n.802+1G>C
ENST00000368984.7:c.1120+1G>C ENSP00000357980.3:n.1120+1G>C
ENST00000420892.1:c.343+1G>C ENSP00000412676.1:n.343+1G>C
NM_002775.4:c.1120+1G>C NP_002766.1:n.1120+1G>C
NM_002775.5:c.1120+1G>C MANE Select NP_002766.1:n.1120+1G>C
Search 100 bp 5'
Search 100 bp 3'