Canonical Allele Identifier: CA305199241

Gene: P2RY11 PPAN-P2RY11

Linked Data

• dbSNP Id: rs973725142
• gnomAD v3: 19-10114816-T-G
• gnomAD v4: 19-10114816-T-G
• MyVariant Identifiers: chr19:g.10225492T>G (hg19) ; chr19:g.10114816T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10114816T>G , CM000681.2:g.10114816T>G	GRCh38
NC_000019.9:g.10225492T>G , CM000681.1:g.10225492T>G	GRCh37
NC_000019.8:g.10086492T>G	NCBI36
NG_047007.1:g.8296T>G
NG_051197.1:g.10109A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321826.5:c.*78T>G (P2RY11) MANE Select	ENSP00000323872.4:n.*78T>G
ENST00000321826.4:c.*78T>G (P2RY11)	ENSP00000323872.4:n.*78T>G
NM_001040664.2:c.*78T>G (PPAN-P2RY11)	NP_001035754.1:n.*78T>G
NM_001198690.1:c.*962T>G (PPAN-P2RY11)	NP_001185619.1:n.*962T>G
NM_002566.4:c.*78T>G (P2RY11)	NP_002557.2:n.*78T>G
NM_002566.5:c.*78T>G (P2RY11) MANE Select	NP_002557.2:n.*78T>G
NM_001040664.3:c.*78T>G (PPAN-P2RY11)	NP_001035754.1:n.*78T>G
NM_001198690.2:c.*962T>G (PPAN-P2RY11)	NP_001185619.1:n.*962T>G