Canonical Allele Identifier: CA305199326
Gene: P2RY11 HGNC NCBI
PPAN-P2RY11 HGNC NCBI

Linked Data

dbSNP Id: rs544895911
gnomAD v2: 19-10225564-C-G
gnomAD v3: 19-10114888-C-G
gnomAD v4: 19-10114888-C-G
MyVariant Identifiers: chr19:g.10225564C>G (hg19) chr19:g.10114888C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10114888C>G , CM000681.2:g.10114888C>G GRCh38
NC_000019.9:g.10225564C>G , CM000681.1:g.10225564C>G GRCh37
NC_000019.8:g.10086564C>G NCBI36
NG_047007.1:g.8368C>G
NG_051197.1:g.10037G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000321826.5:c.*150C>G (P2RY11) MANE Select ENSP00000323872.4:n.*150C>G
ENST00000321826.4:c.*150C>G (P2RY11) ENSP00000323872.4:n.*150C>G
NM_001040664.2:c.*150C>G (PPAN-P2RY11) NP_001035754.1:n.*150C>G
NM_001198690.1:c.*1034C>G (PPAN-P2RY11) NP_001185619.1:n.*1034C>G
NM_002566.4:c.*150C>G (P2RY11) NP_002557.2:n.*150C>G
NM_002566.5:c.*150C>G (P2RY11) MANE Select NP_002557.2:n.*150C>G
NM_001040664.3:c.*150C>G (PPAN-P2RY11) NP_001035754.1:n.*150C>G
NM_001198690.2:c.*1034C>G (PPAN-P2RY11) NP_001185619.1:n.*1034C>G
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