Canonical Allele Identifier: CA305199265

Gene: P2RY11 PPAN-P2RY11

Linked Data

• dbSNP Id: rs919043062
• gnomAD v2: 19-10225526-G-C
• gnomAD v3: 19-10114850-G-C
• gnomAD v4: 19-10114850-G-C
• MyVariant Identifiers: chr19:g.10225526G>C (hg19) ; chr19:g.10114850G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10114850G>C , CM000681.2:g.10114850G>C	GRCh38
NC_000019.9:g.10225526G>C , CM000681.1:g.10225526G>C	GRCh37
NC_000019.8:g.10086526G>C	NCBI36
NG_047007.1:g.8330G>C
NG_051197.1:g.10075C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321826.5:c.*112G>C (P2RY11) MANE Select	ENSP00000323872.4:n.*112G>C
ENST00000321826.4:c.*112G>C (P2RY11)	ENSP00000323872.4:n.*112G>C
NM_001040664.2:c.*112G>C (PPAN-P2RY11)	NP_001035754.1:n.*112G>C
NM_001198690.1:c.*996G>C (PPAN-P2RY11)	NP_001185619.1:n.*996G>C
NM_002566.4:c.*112G>C (P2RY11)	NP_002557.2:n.*112G>C
NM_002566.5:c.*112G>C (P2RY11) MANE Select	NP_002557.2:n.*112G>C
NM_001040664.3:c.*112G>C (PPAN-P2RY11)	NP_001035754.1:n.*112G>C
NM_001198690.2:c.*996G>C (PPAN-P2RY11)	NP_001185619.1:n.*996G>C