Canonical Allele Identifier: CA378606136
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1346234221
gnomAD v2: 10-124221473-G-A
gnomAD v4: 10-122461957-G-A
MyVariant Identifiers: chr10:g.124221473G>A (hg19) chr10:g.122461957G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461957G>A , CM000672.2:g.122461957G>A GRCh38
NC_000010.10:g.124221473G>A , CM000672.1:g.124221473G>A GRCh37
NC_000010.9:g.124211463G>A NCBI36
NG_011554.1:g.5433G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.305G>A MANE Select ENSP00000357980.3:p.Arg102Gln
ENST00000648167.1:c.154+3248G>A ENSP00000498033.1:n.154+3248G>A
ENST00000368984.7:c.305G>A ENSP00000357980.3:p.Arg102Gln
NM_002775.4:c.305G>A NP_002766.1:p.Arg102Gln
NM_002775.5:c.305G>A MANE Select NP_002766.1:p.Arg102Gln
Search 100 bp 5'
Search 100 bp 3'