Canonical Allele Identifier: CA2611238799
Gene: HTRA1 HGNC NCBI

Linked Data

gnomAD v4: 10-122461606-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461606C>A , CM000672.2:g.122461606C>A GRCh38
NC_000010.10:g.124221122C>A , CM000672.1:g.124221122C>A GRCh37
NC_000010.9:g.124211112C>A NCBI36
NG_011554.1:g.5082C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.-47C>A MANE Select ENSP00000357980.3:n.-47C>A
ENST00000648167.1:c.154+2897C>A ENSP00000498033.1:n.154+2897C>A
ENST00000368984.7:c.-47C>A ENSP00000357980.3:n.-47C>A
NM_002775.4:c.-47C>A NP_002766.1:n.-47C>A
NM_002775.5:c.-47C>A MANE Select NP_002766.1:n.-47C>A
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