Canonical Allele Identifier: CA631444908

Gene: P2RY11 PPAN-P2RY11

Linked Data

• dbSNP Id: rs1176349365
• gnomAD v2: 19-10225573-C-T
• gnomAD v3: 19-10114897-C-T
• gnomAD v4: 19-10114897-C-T
• MyVariant Identifiers: chr19:g.10225573C>T (hg19) ; chr19:g.10114897C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10114897C>T , CM000681.2:g.10114897C>T	GRCh38
NC_000019.9:g.10225573C>T , CM000681.1:g.10225573C>T	GRCh37
NC_000019.8:g.10086573C>T	NCBI36
NG_047007.1:g.8377C>T
NG_051197.1:g.10028G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321826.5:c.*159C>T (P2RY11) MANE Select	ENSP00000323872.4:n.*159C>T
ENST00000321826.4:c.*159C>T (P2RY11)	ENSP00000323872.4:n.*159C>T
NM_001040664.2:c.*159C>T (PPAN-P2RY11)	NP_001035754.1:n.*159C>T
NM_001198690.1:c.*1043C>T (PPAN-P2RY11)	NP_001185619.1:n.*1043C>T
NM_002566.4:c.*159C>T (P2RY11)	NP_002557.2:n.*159C>T
NM_002566.5:c.*159C>T (P2RY11) MANE Select	NP_002557.2:n.*159C>T
NM_001040664.3:c.*159C>T (PPAN-P2RY11)	NP_001035754.1:n.*159C>T
NM_001198690.2:c.*1043C>T (PPAN-P2RY11)	NP_001185619.1:n.*1043C>T