Canonical Allele Identifier: CA607882470

Gene: P2RX7

Linked Data

• dbSNP Id: rs1403708094
• gnomAD v2: 12-121570762-G-A
• gnomAD v4: 12-121132959-G-A
• MyVariant Identifiers: chr12:g.121570762G>A (hg19) ; chr12:g.121132959G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121132959G>A , CM000674.2:g.121132959G>A	GRCh38
NC_000012.11:g.121570762G>A , CM000674.1:g.121570762G>A	GRCh37
NC_000012.10:g.120055145G>A	NCBI36
NG_011471.2:g.5085G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.-12G>A MANE Select	ENSP00000330696.6:n.-12G>A
ENST00000261826.10:c.-12G>A	ENSP00000261826.6:n.-12G>A
ENST00000328963.9:c.-12G>A	ENSP00000330696.6:n.-12G>A
ENST00000535928.5:c.-12G>A	ENSP00000439961.1:n.-12G>A
ENST00000537312.5:c.-12G>A	ENSP00000438586.1:n.-12G>A
ENST00000539695.5:n.58G>A
ENST00000545434.5:c.-12G>A	ENSP00000445564.1:n.-12G>A
NM_002562.5:c.-12G>A	NP_002553.3:n.-12G>A
NR_033948.1:n.132G>A
NR_033949.1:n.132G>A
NR_033950.1:n.132G>A
NR_033951.1:n.132G>A
NR_033952.1:n.132G>A
NR_033953.1:n.141G>A
NR_033954.1:n.132G>A
NR_033955.1:n.132G>A
NR_033956.1:n.132G>A
XM_011538418.1:c.-12G>A	XP_011536720.1:n.-12G>A
XM_011538419.1:c.-155G>A	XP_011536721.1:n.-155G>A
XM_011538419.3:c.-155G>A	XP_011536721.1:n.-155G>A
XM_017019364.2:c.-525G>A	XP_016874853.1:n.-525G>A
XM_017019365.2:c.-356G>A	XP_016874854.1:n.-356G>A
XM_017019366.2:c.-692G>A	XP_016874855.1:n.-692G>A
XM_017019367.2:c.-523G>A	XP_016874856.1:n.-523G>A
XR_001749352.2:n.187-6118C>T
XR_001749354.2:n.187-6118C>T
NM_002562.6:c.-12G>A MANE Select	NP_002553.3:n.-12G>A
NR_033948.2:n.84G>A
NR_033949.2:n.84G>A
NR_033950.2:n.84G>A
NR_033951.2:n.84G>A
NR_033952.2:n.84G>A
NR_033953.2:n.84G>A
NR_033954.2:n.84G>A
NR_033955.2:n.84G>A
NR_033956.2:n.84G>A