Canonical Allele Identifier: CA1941477123
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs2097503141
gnomAD v4: 10-122506562-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506562A>G , CM000672.2:g.122506562A>G GRCh38
NC_000010.10:g.124266078A>G , CM000672.1:g.124266078A>G GRCh37
NC_000010.9:g.124256068A>G NCBI36
NG_011554.1:g.50038A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.778-129A>G MANE Select ENSP00000357980.3:n.778-129A>G
ENST00000648167.1:c.460-129A>G ENSP00000498033.1:n.460-129A>G
ENST00000368984.7:c.778-129A>G ENSP00000357980.3:n.778-129A>G
NM_002775.4:c.778-129A>G NP_002766.1:n.778-129A>G
NM_002775.5:c.778-129A>G MANE Select NP_002766.1:n.778-129A>G
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