Canonical Allele Identifier: CA471666585
Gene: HTRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.124266221C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506705C>G , CM000672.2:g.122506705C>G GRCh38
NC_000010.10:g.124266221C>G , CM000672.1:g.124266221C>G GRCh37
NC_000010.9:g.124256211C>G NCBI36
NG_011554.1:g.50181C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.792C>G MANE Select ENSP00000357980.3:p.Val264=
ENST00000648167.1:c.474C>G ENSP00000498033.1:p.Val158=
ENST00000368984.7:c.792C>G ENSP00000357980.3:p.Val264=
ENST00000420892.1:c.15C>G ENSP00000412676.1:p.Val5=
NM_002775.4:c.792C>G NP_002766.1:p.Val264=
NM_002775.5:c.792C>G MANE Select NP_002766.1:p.Val264=