Canonical Allele Identifier: CA378585809
Gene: HTRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.124266370T>G (hg19) chr10:g.122506854T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506854T>G , CM000672.2:g.122506854T>G GRCh38
NC_000010.10:g.124266370T>G , CM000672.1:g.124266370T>G GRCh37
NC_000010.9:g.124256360T>G NCBI36
NG_011554.1:g.50330T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.941T>G MANE Select ENSP00000357980.3:p.Met314Arg
ENST00000648167.1:c.623T>G ENSP00000498033.1:p.Met208Arg
ENST00000368984.7:c.941T>G ENSP00000357980.3:p.Met314Arg
ENST00000420892.1:c.164T>G ENSP00000412676.1:p.Met55Arg
NM_002775.4:c.941T>G NP_002766.1:p.Met314Arg
NM_002775.5:c.941T>G MANE Select NP_002766.1:p.Met314Arg
Search 100 bp 5'
Search 100 bp 3'