Canonical Allele Identifier: CA471666869
Gene: HTRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.124266305C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506789C>T , CM000672.2:g.122506789C>T GRCh38
NC_000010.10:g.124266305C>T , CM000672.1:g.124266305C>T GRCh37
NC_000010.9:g.124256295C>T NCBI36
NG_011554.1:g.50265C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.876C>T MANE Select ENSP00000357980.3:p.Val292=
ENST00000648167.1:c.558C>T ENSP00000498033.1:p.Val186=
ENST00000368984.7:c.876C>T ENSP00000357980.3:p.Val292=
ENST00000420892.1:c.99C>T ENSP00000412676.1:p.Val33=
NM_002775.4:c.876C>T NP_002766.1:p.Val292=
NM_002775.5:c.876C>T MANE Select NP_002766.1:p.Val292=