Canonical Allele Identifier: CA993413320
Gene: P2RY11 HGNC NCBI
PPAN-P2RY11 HGNC NCBI

Linked Data

dbSNP Id: rs2089212891

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10114985C>G , CM000681.2:g.10114985C>G GRCh38
NC_000019.9:g.10225661C>G , CM000681.1:g.10225661C>G GRCh37
NC_000019.8:g.10086661C>G NCBI36
NG_047007.1:g.8465C>G
NG_051197.1:g.9940G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000321826.5:c.*247C>G (P2RY11) MANE Select ENSP00000323872.4:n.*247C>G
ENST00000321826.4:c.*247C>G (P2RY11) ENSP00000323872.4:n.*247C>G
NM_001040664.2:c.*247C>G (PPAN-P2RY11) NP_001035754.1:n.*247C>G
NM_001198690.1:c.*1131C>G (PPAN-P2RY11) NP_001185619.1:n.*1131C>G
NM_002566.4:c.*247C>G (P2RY11) NP_002557.2:n.*247C>G
NM_002566.5:c.*247C>G (P2RY11) MANE Select NP_002557.2:n.*247C>G
NM_001040664.3:c.*247C>G (PPAN-P2RY11) NP_001035754.1:n.*247C>G
NM_001198690.2:c.*1131C>G (PPAN-P2RY11) NP_001185619.1:n.*1131C>G