Canonical Allele Identifier: CA13486800

Gene: P2RY2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.73238127G>A , CM000673.2:g.73238127G>A	GRCh38
NC_000011.9:g.72949172G>A , CM000673.1:g.72949172G>A	GRCh37
NC_000011.8:g.72626820G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393597.7:c.*2834G>A MANE Select	ENSP00000377222.2:n.*2834G>A
NM_002564.3:c.*2834G>A	NP_002555.3:n.*2834G>A
NM_176071.2:c.*2834G>A	NP_788085.2:n.*2834G>A
NM_176072.2:c.*2834G>A	NP_788086.2:n.*2834G>A
XR_001747890.1:n.1933+2387G>A
XR_001747891.1:n.1933+2387G>A
XR_001747892.1:n.1933+2387G>A
NM_002564.4:c.*2834G>A MANE Select	NP_002555.4:n.*2834G>A
NM_176071.3:c.*2834G>A	NP_788085.3:n.*2834G>A
NM_176072.3:c.*2834G>A	NP_788086.3:n.*2834G>A