Canonical Allele Identifier: CA993413335
Gene: P2RY11 HGNC NCBI
PPAN-P2RY11 HGNC NCBI

Linked Data

dbSNP Id: rs2089213326

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115000C>T , CM000681.2:g.10115000C>T GRCh38
NC_000019.9:g.10225676C>T , CM000681.1:g.10225676C>T GRCh37
NC_000019.8:g.10086676C>T NCBI36
NG_047007.1:g.8480C>T
NG_051197.1:g.9925G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000321826.5:c.*262C>T (P2RY11) MANE Select ENSP00000323872.4:n.*262C>T
ENST00000321826.4:c.*262C>T (P2RY11) ENSP00000323872.4:n.*262C>T
NM_001040664.2:c.*262C>T (PPAN-P2RY11) NP_001035754.1:n.*262C>T
NM_001198690.1:c.*1146C>T (PPAN-P2RY11) NP_001185619.1:n.*1146C>T
NM_002566.4:c.*262C>T (P2RY11) NP_002557.2:n.*262C>T
NM_002566.5:c.*262C>T (P2RY11) MANE Select NP_002557.2:n.*262C>T
NM_001040664.3:c.*262C>T (PPAN-P2RY11) NP_001035754.1:n.*262C>T
NM_001198690.2:c.*1146C>T (PPAN-P2RY11) NP_001185619.1:n.*1146C>T