Canonical Allele Identifier: CA378586664
Gene: HTRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.124268232C>G (hg19) chr10:g.122508716C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508716C>G , CM000672.2:g.122508716C>G GRCh38
NC_000010.10:g.124268232C>G , CM000672.1:g.124268232C>G GRCh37
NC_000010.9:g.124258222C>G NCBI36
NG_011554.1:g.52192C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1066C>G MANE Select ENSP00000357980.3:p.Pro356Ala
ENST00000648167.1:c.748C>G ENSP00000498033.1:p.Pro250Ala
ENST00000368984.7:c.1066C>G ENSP00000357980.3:p.Pro356Ala
ENST00000420892.1:c.289C>G ENSP00000412676.1:p.Pro97Ala
NM_002775.4:c.1066C>G NP_002766.1:p.Pro356Ala
NM_002775.5:c.1066C>G MANE Select NP_002766.1:p.Pro356Ala
Search 100 bp 5'
Search 100 bp 3'