Canonical Allele Identifier: CA5726052
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs369953066
ExAC: 10:124268321 A / C
gnomAD v2: 10-124268321-A-C
gnomAD v3: 10-122508805-A-C
gnomAD v4: 10-122508805-A-C
MyVariant Identifiers: chr10:g.124268321A>C (hg19) chr10:g.122508805A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508805A>C , CM000672.2:g.122508805A>C GRCh38
NC_000010.10:g.124268321A>C , CM000672.1:g.124268321A>C GRCh37
NC_000010.9:g.124258311A>C NCBI36
NG_011554.1:g.52281A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1120+35A>C MANE Select ENSP00000357980.3:n.1120+35A>C
ENST00000648167.1:c.802+35A>C ENSP00000498033.1:n.802+35A>C
ENST00000368984.7:c.1120+35A>C ENSP00000357980.3:n.1120+35A>C
ENST00000420892.1:c.343+35A>C ENSP00000412676.1:n.343+35A>C
NM_002775.4:c.1120+35A>C NP_002766.1:n.1120+35A>C
NM_002775.5:c.1120+35A>C MANE Select NP_002766.1:n.1120+35A>C
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