Canonical Allele Identifier: CA2322269818
Gene: P2RY11 HGNC NCBI
PPAN-P2RY11 HGNC NCBI

Linked Data

dbSNP Id: rs1468524552

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10114832G>C , CM000681.2:g.10114832G>C GRCh38
NC_000019.9:g.10225508G>C , CM000681.1:g.10225508G>C GRCh37
NC_000019.8:g.10086508G>C NCBI36
NG_047007.1:g.8312G>C
NG_051197.1:g.10093C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000321826.5:c.*94G>C (P2RY11) MANE Select ENSP00000323872.4:n.*94G>C
ENST00000321826.4:c.*94G>C (P2RY11) ENSP00000323872.4:n.*94G>C
NM_001040664.2:c.*94G>C (PPAN-P2RY11) NP_001035754.1:n.*94G>C
NM_001198690.1:c.*978G>C (PPAN-P2RY11) NP_001185619.1:n.*978G>C
NM_002566.4:c.*94G>C (P2RY11) NP_002557.2:n.*94G>C
NM_002566.5:c.*94G>C (P2RY11) MANE Select NP_002557.2:n.*94G>C
NM_001040664.3:c.*94G>C (PPAN-P2RY11) NP_001035754.1:n.*94G>C
NM_001198690.2:c.*978G>C (PPAN-P2RY11) NP_001185619.1:n.*978G>C