Canonical Allele Identifier: CA305199252

Gene: P2RY11 PPAN-P2RY11

Linked Data

• dbSNP Id: rs973062822
• gnomAD v2: 19-10225498-C-A
• gnomAD v3: 19-10114822-C-A
• gnomAD v4: 19-10114822-C-A
• MyVariant Identifiers: chr19:g.10225498C>A (hg19) ; chr19:g.10114822C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10114822C>A , CM000681.2:g.10114822C>A	GRCh38
NC_000019.9:g.10225498C>A , CM000681.1:g.10225498C>A	GRCh37
NC_000019.8:g.10086498C>A	NCBI36
NG_047007.1:g.8302C>A
NG_051197.1:g.10103G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321826.5:c.*84C>A (P2RY11) MANE Select	ENSP00000323872.4:n.*84C>A
ENST00000321826.4:c.*84C>A (P2RY11)	ENSP00000323872.4:n.*84C>A
NM_001040664.2:c.*84C>A (PPAN-P2RY11)	NP_001035754.1:n.*84C>A
NM_001198690.1:c.*968C>A (PPAN-P2RY11)	NP_001185619.1:n.*968C>A
NM_002566.4:c.*84C>A (P2RY11)	NP_002557.2:n.*84C>A
NM_002566.5:c.*84C>A (P2RY11) MANE Select	NP_002557.2:n.*84C>A
NM_001040664.3:c.*84C>A (PPAN-P2RY11)	NP_001035754.1:n.*84C>A
NM_001198690.2:c.*968C>A (PPAN-P2RY11)	NP_001185619.1:n.*968C>A