Canonical Allele Identifier: CA214415455
Gene: HTRA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1441450
ClinVar RCV Id: RCV001950641 RCV002562793
dbSNP Id: rs952385517
gnomAD v2: 10-124221602-C-A
gnomAD v3: 10-122462086-C-A
gnomAD v4: 10-122462086-C-A
MyVariant Identifiers: chr10:g.124221602C>A (hg19) chr10:g.122462086C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122462086C>A , CM000672.2:g.122462086C>A GRCh38
NC_000010.10:g.124221602C>A , CM000672.1:g.124221602C>A GRCh37
NC_000010.9:g.124211592C>A NCBI36
NG_011554.1:g.5562C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.434C>A MANE Select ENSP00000357980.3:p.Pro145Gln
ENST00000648167.1:c.154+3377C>A ENSP00000498033.1:n.154+3377C>A
ENST00000368984.7:c.434C>A ENSP00000357980.3:p.Pro145Gln
NM_002775.4:c.434C>A NP_002766.1:p.Pro145Gln
NM_002775.5:c.434C>A MANE Select NP_002766.1:p.Pro145Gln
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