Canonical Allele Identifier: CA2611238735
Gene: HTRA1 HGNC NCBI

Linked Data

gnomAD v4: 10-122461576-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461576C>G , CM000672.2:g.122461576C>G GRCh38
NC_000010.10:g.124221092C>G , CM000672.1:g.124221092C>G GRCh37
NC_000010.9:g.124211082C>G NCBI36
NG_011554.1:g.5052C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.-77C>G MANE Select ENSP00000357980.3:n.-77C>G
ENST00000648167.1:c.154+2867C>G ENSP00000498033.1:n.154+2867C>G
ENST00000368984.7:c.-77C>G ENSP00000357980.3:n.-77C>G
NM_002775.4:c.-77C>G NP_002766.1:n.-77C>G
NM_002775.5:c.-77C>G MANE Select NP_002766.1:n.-77C>G
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