Canonical Allele Identifier: CA214412786
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1050164254
MyVariant Identifiers: chr10:g.124268478C>G (hg19) chr10:g.122508962C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508962C>G , CM000672.2:g.122508962C>G GRCh38
NC_000010.10:g.124268478C>G , CM000672.1:g.124268478C>G GRCh37
NC_000010.9:g.124258468C>G NCBI36
NG_011554.1:g.52438C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1120+192C>G MANE Select ENSP00000357980.3:n.1120+192C>G
ENST00000648167.1:c.802+192C>G ENSP00000498033.1:n.802+192C>G
ENST00000368984.7:c.1120+192C>G ENSP00000357980.3:n.1120+192C>G
ENST00000420892.1:c.343+192C>G ENSP00000412676.1:n.343+192C>G
NM_002775.4:c.1120+192C>G NP_002766.1:n.1120+192C>G
NM_002775.5:c.1120+192C>G MANE Select NP_002766.1:n.1120+192C>G
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