Canonical Allele Identifier: CA660910951
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1426914368
gnomAD v3: 10-122507211-A-AT
gnomAD v4: 10-122507211-A-AT
MyVariant Identifiers: chr10:g.124266727_124266728insT (hg19) chr10:g.122507211_122507212insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122507218dup , CM000672.2:g.122507218dup GRCh38
NC_000010.10:g.124266734dup , CM000672.1:g.124266734dup GRCh37
NC_000010.9:g.124256724dup NCBI36
NG_011554.1:g.50694dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.973-152dup MANE Select ENSP00000357980.3:n.973-152dup
ENST00000648167.1:c.655-152dup ENSP00000498033.1:n.655-152dup
ENST00000368984.7:c.973-152dup ENSP00000357980.3:n.973-152dup
ENST00000420892.1:c.196-152dup ENSP00000412676.1:n.196-152dup
NM_002775.4:c.973-152dup NP_002766.1:n.973-152dup
NM_002775.5:c.973-152dup MANE Select NP_002766.1:n.973-152dup
Search 100 bp 5'
Search 100 bp 3'