Canonical Allele Identifier: CA660865465
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1184223007
gnomAD v3: 10-122461499-A-C
gnomAD v4: 10-122461499-A-C
MyVariant Identifiers: chr10:g.124221015A>C (hg19) chr10:g.122461499A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461499A>C , CM000672.2:g.122461499A>C GRCh38
NC_000010.10:g.124221015A>C , CM000672.1:g.124221015A>C GRCh37
NC_000010.9:g.124211005A>C NCBI36
NG_011554.1:g.4975A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000648167.1:c.154+2790A>C ENSP00000498033.1:n.154+2790A>C
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