Canonical Allele Identifier: CA660910947
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1175502445
gnomAD v3: 10-122507190-T-G
gnomAD v4: 10-122507190-T-G
MyVariant Identifiers: chr10:g.124266706T>G (hg19) chr10:g.122507190T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122507190T>G , CM000672.2:g.122507190T>G GRCh38
NC_000010.10:g.124266706T>G , CM000672.1:g.124266706T>G GRCh37
NC_000010.9:g.124256696T>G NCBI36
NG_011554.1:g.50666T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.973-180T>G MANE Select ENSP00000357980.3:n.973-180T>G
ENST00000648167.1:c.655-180T>G ENSP00000498033.1:n.655-180T>G
ENST00000368984.7:c.973-180T>G ENSP00000357980.3:n.973-180T>G
ENST00000420892.1:c.196-180T>G ENSP00000412676.1:n.196-180T>G
NM_002775.4:c.973-180T>G NP_002766.1:n.973-180T>G
NM_002775.5:c.973-180T>G MANE Select NP_002766.1:n.973-180T>G
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