Canonical Allele Identifier: CA471666557
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1565433817
gnomAD v4: 10-122506697-C-T
MyVariant Identifiers: chr10:g.124266213C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506697C>T , CM000672.2:g.122506697C>T GRCh38
NC_000010.10:g.124266213C>T , CM000672.1:g.124266213C>T GRCh37
NC_000010.9:g.124256203C>T NCBI36
NG_011554.1:g.50173C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.784C>T MANE Select ENSP00000357980.3:p.Leu262=
ENST00000648167.1:c.466C>T ENSP00000498033.1:p.Leu156=
ENST00000368984.7:c.784C>T ENSP00000357980.3:p.Leu262=
ENST00000420892.1:c.7C>T ENSP00000412676.1:p.Leu3=
NM_002775.4:c.784C>T NP_002766.1:p.Leu262=
NM_002775.5:c.784C>T MANE Select NP_002766.1:p.Leu262=
Search 100 bp 5'
Search 100 bp 3'