Canonical Allele Identifier: CA1941459048
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs2097481193
gnomAD v4: 10-122461528-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461528T>G , CM000672.2:g.122461528T>G GRCh38
NC_000010.10:g.124221044T>G , CM000672.1:g.124221044T>G GRCh37
NC_000010.9:g.124211034T>G NCBI36
NG_011554.1:g.5004T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648167.1:c.154+2819T>G ENSP00000498033.1:n.154+2819T>G
ENST00000368984.7:c.-125T>G ENSP00000357980.3:n.-125T>G
NM_002775.4:c.-125T>G NP_002766.1:n.-125T>G
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