Canonical Allele Identifier: CA660871735
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1200280885
MyVariant Identifiers: chr10:g.124231757T>A (hg19) chr10:g.122472241T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122472241T>A , CM000672.2:g.122472241T>A GRCh38
NC_000010.10:g.124231757T>A , CM000672.1:g.124231757T>A GRCh37
NC_000010.9:g.124221747T>A NCBI36
NG_011554.1:g.15717T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.472+10117T>A MANE Select ENSP00000357980.3:n.472+10117T>A
ENST00000648167.1:c.154+13532T>A ENSP00000498033.1:n.154+13532T>A
ENST00000368984.7:c.472+10117T>A ENSP00000357980.3:n.472+10117T>A
NM_002775.4:c.472+10117T>A NP_002766.1:n.472+10117T>A
NM_002775.5:c.472+10117T>A MANE Select NP_002766.1:n.472+10117T>A
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