Canonical Allele Identifier: CA2621395754

Gene: P2RX7

Linked Data

• gnomAD v4: 12-121132915-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121132915C>A , CM000674.2:g.121132915C>A	GRCh38
NC_000012.11:g.121570718C>A , CM000674.1:g.121570718C>A	GRCh37
NC_000012.10:g.120055101C>A	NCBI36
NG_011471.2:g.5041C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.-56C>A MANE Select	ENSP00000330696.6:n.-56C>A
ENST00000328963.9:c.-56C>A	ENSP00000330696.6:n.-56C>A
ENST00000535928.5:c.-56C>A	ENSP00000439961.1:n.-56C>A
ENST00000537312.5:c.-56C>A	ENSP00000438586.1:n.-56C>A
ENST00000539695.5:n.14C>A
NM_002562.5:c.-56C>A	NP_002553.3:n.-56C>A
NR_033948.1:n.88C>A
NR_033949.1:n.88C>A
NR_033950.1:n.88C>A
NR_033951.1:n.88C>A
NR_033952.1:n.88C>A
NR_033953.1:n.97C>A
NR_033954.1:n.88C>A
NR_033955.1:n.88C>A
NR_033956.1:n.88C>A
XM_011538418.1:c.-56C>A	XP_011536720.1:n.-56C>A
XM_011538419.1:c.-199C>A	XP_011536721.1:n.-199C>A
XM_011538419.3:c.-199C>A	XP_011536721.1:n.-199C>A
XM_017019364.2:c.-569C>A	XP_016874853.1:n.-569C>A
XM_017019366.2:c.-736C>A	XP_016874855.1:n.-736C>A
XM_017019367.2:c.-567C>A	XP_016874856.1:n.-567C>A
XR_001749352.2:n.187-6074G>T
XR_001749354.2:n.187-6074G>T
NM_002562.6:c.-56C>A MANE Select	NP_002553.3:n.-56C>A
NR_033948.2:n.40C>A
NR_033949.2:n.40C>A
NR_033950.2:n.40C>A
NR_033951.2:n.40C>A
NR_033952.2:n.40C>A
NR_033953.2:n.40C>A
NR_033954.2:n.40C>A
NR_033955.2:n.40C>A
NR_033956.2:n.40C>A