Canonical Allele Identifier: CA2611239015
Gene: HTRA1 HGNC NCBI

Linked Data

gnomAD v4: 10-122461645-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461645G>C , CM000672.2:g.122461645G>C GRCh38
NC_000010.10:g.124221161G>C , CM000672.1:g.124221161G>C GRCh37
NC_000010.9:g.124211151G>C NCBI36
NG_011554.1:g.5121G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.-8G>C MANE Select ENSP00000357980.3:n.-8G>C
ENST00000648167.1:c.154+2936G>C ENSP00000498033.1:n.154+2936G>C
ENST00000368984.7:c.-8G>C ENSP00000357980.3:n.-8G>C
NM_002775.4:c.-8G>C NP_002766.1:n.-8G>C
NM_002775.5:c.-8G>C MANE Select NP_002766.1:n.-8G>C
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