Canonical Allele Identifier: CA378586399
Gene: HTRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.124268187G>A (hg19) chr10:g.122508671G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508671G>A , CM000672.2:g.122508671G>A GRCh38
NC_000010.10:g.124268187G>A , CM000672.1:g.124268187G>A GRCh37
NC_000010.9:g.124258177G>A NCBI36
NG_011554.1:g.52147G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.1021G>A MANE Select ENSP00000357980.3:p.Gly341Arg
ENST00000648167.1:c.703G>A ENSP00000498033.1:p.Gly235Arg
ENST00000368984.7:c.1021G>A ENSP00000357980.3:p.Gly341Arg
ENST00000420892.1:c.244G>A ENSP00000412676.1:p.Gly82Arg
NM_002775.4:c.1021G>A NP_002766.1:p.Gly341Arg
NM_002775.5:c.1021G>A MANE Select NP_002766.1:p.Gly341Arg
Search 100 bp 5'
Search 100 bp 3'