Canonical Allele Identifier: CA378585771
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs2097503252
gnomAD v4: 10-122506835-G-A
MyVariant Identifiers: chr10:g.124266351G>A (hg19) chr10:g.122506835G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506835G>A , CM000672.2:g.122506835G>A GRCh38
NC_000010.10:g.124266351G>A , CM000672.1:g.124266351G>A GRCh37
NC_000010.9:g.124256341G>A NCBI36
NG_011554.1:g.50311G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.922G>A MANE Select ENSP00000357980.3:p.Gly308Arg
ENST00000648167.1:c.604G>A ENSP00000498033.1:p.Gly202Arg
ENST00000368984.7:c.922G>A ENSP00000357980.3:p.Gly308Arg
ENST00000420892.1:c.145G>A ENSP00000412676.1:p.Gly49Arg
NM_002775.4:c.922G>A NP_002766.1:p.Gly308Arg
NM_002775.5:c.922G>A MANE Select NP_002766.1:p.Gly308Arg
Search 100 bp 5'
Search 100 bp 3'