Canonical Allele Identifier: CA596578952
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1458253836
gnomAD v2: 10-124221047-G-A
gnomAD v4: 10-122461531-G-A
MyVariant Identifiers: chr10:g.124221047G>A (hg19) chr10:g.122461531G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461531G>A , CM000672.2:g.122461531G>A GRCh38
NC_000010.10:g.124221047G>A , CM000672.1:g.124221047G>A GRCh37
NC_000010.9:g.124211037G>A NCBI36
NG_011554.1:g.5007G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648167.1:c.154+2822G>A ENSP00000498033.1:n.154+2822G>A
ENST00000368984.7:c.-122G>A ENSP00000357980.3:n.-122G>A
NM_002775.4:c.-122G>A NP_002766.1:n.-122G>A
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