Canonical Allele Identifier: CA783165582

Gene: P2RY11 PPAN-P2RY11

Linked Data

• dbSNP Id: rs1454228326
• gnomAD v3: 19-10114875-A-C
• gnomAD v4: 19-10114875-A-C
• MyVariant Identifiers: chr19:g.10225551A>C (hg19) ; chr19:g.10114875A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10114875A>C , CM000681.2:g.10114875A>C	GRCh38
NC_000019.9:g.10225551A>C , CM000681.1:g.10225551A>C	GRCh37
NC_000019.8:g.10086551A>C	NCBI36
NG_047007.1:g.8355A>C
NG_051197.1:g.10050T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321826.5:c.*137A>C (P2RY11) MANE Select	ENSP00000323872.4:n.*137A>C
ENST00000321826.4:c.*137A>C (P2RY11)	ENSP00000323872.4:n.*137A>C
NM_001040664.2:c.*137A>C (PPAN-P2RY11)	NP_001035754.1:n.*137A>C
NM_001198690.1:c.*1021A>C (PPAN-P2RY11)	NP_001185619.1:n.*1021A>C
NM_002566.4:c.*137A>C (P2RY11)	NP_002557.2:n.*137A>C
NM_002566.5:c.*137A>C (P2RY11) MANE Select	NP_002557.2:n.*137A>C
NM_001040664.3:c.*137A>C (PPAN-P2RY11)	NP_001035754.1:n.*137A>C
NM_001198690.2:c.*1021A>C (PPAN-P2RY11)	NP_001185619.1:n.*1021A>C