Canonical Allele Identifier: CA2621395769

Gene: P2RX7

Linked Data

• dbSNP Id: rs1322150012
• gnomAD v4: 12-121132952-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121132952A>G , CM000674.2:g.121132952A>G	GRCh38
NC_000012.11:g.121570755A>G , CM000674.1:g.121570755A>G	GRCh37
NC_000012.10:g.120055138A>G	NCBI36
NG_011471.2:g.5078A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.-19A>G MANE Select	ENSP00000330696.6:n.-19A>G
ENST00000261826.10:c.-19A>G	ENSP00000261826.6:n.-19A>G
ENST00000328963.9:c.-19A>G	ENSP00000330696.6:n.-19A>G
ENST00000535928.5:c.-19A>G	ENSP00000439961.1:n.-19A>G
ENST00000537312.5:c.-19A>G	ENSP00000438586.1:n.-19A>G
ENST00000539695.5:n.51A>G
ENST00000545434.5:c.-19A>G	ENSP00000445564.1:n.-19A>G
NM_002562.5:c.-19A>G	NP_002553.3:n.-19A>G
NR_033948.1:n.125A>G
NR_033949.1:n.125A>G
NR_033950.1:n.125A>G
NR_033951.1:n.125A>G
NR_033952.1:n.125A>G
NR_033953.1:n.134A>G
NR_033954.1:n.125A>G
NR_033955.1:n.125A>G
NR_033956.1:n.125A>G
XM_011538418.1:c.-19A>G	XP_011536720.1:n.-19A>G
XM_011538419.1:c.-162A>G	XP_011536721.1:n.-162A>G
XM_011538419.3:c.-162A>G	XP_011536721.1:n.-162A>G
XM_017019364.2:c.-532A>G	XP_016874853.1:n.-532A>G
XM_017019365.2:c.-363A>G	XP_016874854.1:n.-363A>G
XM_017019366.2:c.-699A>G	XP_016874855.1:n.-699A>G
XM_017019367.2:c.-530A>G	XP_016874856.1:n.-530A>G
XR_001749352.2:n.187-6111T>C
XR_001749354.2:n.187-6111T>C
NM_002562.6:c.-19A>G MANE Select	NP_002553.3:n.-19A>G
NR_033948.2:n.77A>G
NR_033949.2:n.77A>G
NR_033950.2:n.77A>G
NR_033951.2:n.77A>G
NR_033952.2:n.77A>G
NR_033953.2:n.77A>G
NR_033954.2:n.77A>G
NR_033955.2:n.77A>G
NR_033956.2:n.77A>G