Canonical Allele Identifier: CA1941459027
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs2097481169
gnomAD v4: 10-122461498-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461498C>G , CM000672.2:g.122461498C>G GRCh38
NC_000010.10:g.124221014C>G , CM000672.1:g.124221014C>G GRCh37
NC_000010.9:g.124211004C>G NCBI36
NG_011554.1:g.4974C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648167.1:c.154+2789C>G ENSP00000498033.1:n.154+2789C>G
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