Canonical Allele Identifier: CA471666718
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1591040097
MyVariant Identifiers: chr10:g.124266257A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506741A>G , CM000672.2:g.122506741A>G GRCh38
NC_000010.10:g.124266257A>G , CM000672.1:g.124266257A>G GRCh37
NC_000010.9:g.124256247A>G NCBI36
NG_011554.1:g.50217A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.828A>G MANE Select ENSP00000357980.3:p.Gly276=
ENST00000648167.1:c.510A>G ENSP00000498033.1:p.Gly170=
ENST00000368984.7:c.828A>G ENSP00000357980.3:p.Gly276=
ENST00000420892.1:c.51A>G ENSP00000412676.1:p.Gly17=
NM_002775.4:c.828A>G NP_002766.1:p.Gly276=
NM_002775.5:c.828A>G MANE Select NP_002766.1:p.Gly276=