Canonical Allele Identifier: CA2611246675
Gene: HTRA1 HGNC NCBI

Linked Data

gnomAD v4: 10-122506953-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506953A>G , CM000672.2:g.122506953A>G GRCh38
NC_000010.10:g.124266469A>G , CM000672.1:g.124266469A>G GRCh37
NC_000010.9:g.124256459A>G NCBI36
NG_011554.1:g.50429A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.972+68A>G MANE Select ENSP00000357980.3:n.972+68A>G
ENST00000648167.1:c.654+68A>G ENSP00000498033.1:n.654+68A>G
ENST00000368984.7:c.972+68A>G ENSP00000357980.3:n.972+68A>G
ENST00000420892.1:c.195+68A>G ENSP00000412676.1:n.195+68A>G
NM_002775.4:c.972+68A>G NP_002766.1:n.972+68A>G
NM_002775.5:c.972+68A>G MANE Select NP_002766.1:n.972+68A>G
Search 100 bp 5'
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