Canonical Allele Identifier: CA224795397

Gene: P2RY2

Linked Data

• dbSNP Id: rs903657743
• gnomAD v3: 11-73223591-G-A
• gnomAD v4: 11-73223591-G-A
• MyVariant Identifiers: chr11:g.72934636G>A (hg19) ; chr11:g.73223591G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.73223591G>A , CM000673.2:g.73223591G>A	GRCh38
NC_000011.9:g.72934636G>A , CM000673.1:g.72934636G>A	GRCh37
NC_000011.8:g.72612284G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393597.7:c.-199-4390G>A MANE Select	ENSP00000377222.2:n.-199-4390G>A
ENST00000311131.6:c.-333-4390G>A	ENSP00000310305.2:n.-333-4390G>A
ENST00000393596.2:c.-199-4390G>A	ENSP00000377221.2:n.-199-4390G>A
ENST00000393597.6:c.-199-4390G>A	ENSP00000377222.2:n.-199-4390G>A
NM_002564.3:c.-199-4390G>A	NP_002555.3:n.-199-4390G>A
NM_176071.2:c.-199-4390G>A	NP_788085.2:n.-199-4390G>A
NM_176072.2:c.-333-4390G>A	NP_788086.2:n.-333-4390G>A
XM_005274019.3:c.-199-4390G>A	XP_005274076.1:n.-199-4390G>A
XM_005274020.3:c.-200+2972G>A	XP_005274077.1:n.-200+2972G>A
XM_005274021.3:c.-199-4390G>A	XP_005274078.1:n.-199-4390G>A
XM_011545074.1:c.-199-4390G>A	XP_011543376.1:n.-199-4390G>A
XM_005274019.4:c.-199-4390G>A	XP_005274076.1:n.-199-4390G>A
XM_005274020.4:c.-200+2972G>A	XP_005274077.1:n.-200+2972G>A
XM_005274021.4:c.-199-4390G>A	XP_005274078.1:n.-199-4390G>A
XM_011545074.2:c.-199-4390G>A	XP_011543376.1:n.-199-4390G>A
XM_017017839.1:c.-199-4390G>A	XP_016873328.1:n.-199-4390G>A
XR_001747890.1:n.154-4390G>A
XR_001747891.1:n.154-4390G>A
XR_001747892.1:n.154-4390G>A
NM_002564.4:c.-199-4390G>A MANE Select	NP_002555.4:n.-199-4390G>A
NM_176071.3:c.-199-4390G>A	NP_788085.3:n.-199-4390G>A
NM_176072.3:c.-333-4390G>A	NP_788086.3:n.-333-4390G>A