Canonical Allele Identifier: CA2621395756

Gene: P2RX7

Linked Data

• gnomAD v4: 12-121132922-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121132922G>T , CM000674.2:g.121132922G>T	GRCh38
NC_000012.11:g.121570725G>T , CM000674.1:g.121570725G>T	GRCh37
NC_000012.10:g.120055108G>T	NCBI36
NG_011471.2:g.5048G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.-49G>T MANE Select	ENSP00000330696.6:n.-49G>T
ENST00000328963.9:c.-49G>T	ENSP00000330696.6:n.-49G>T
ENST00000535928.5:c.-49G>T	ENSP00000439961.1:n.-49G>T
ENST00000537312.5:c.-49G>T	ENSP00000438586.1:n.-49G>T
ENST00000539695.5:n.21G>T
NM_002562.5:c.-49G>T	NP_002553.3:n.-49G>T
NR_033948.1:n.95G>T
NR_033949.1:n.95G>T
NR_033950.1:n.95G>T
NR_033951.1:n.95G>T
NR_033952.1:n.95G>T
NR_033953.1:n.104G>T
NR_033954.1:n.95G>T
NR_033955.1:n.95G>T
NR_033956.1:n.95G>T
XM_011538418.1:c.-49G>T	XP_011536720.1:n.-49G>T
XM_011538419.1:c.-192G>T	XP_011536721.1:n.-192G>T
XM_011538419.3:c.-192G>T	XP_011536721.1:n.-192G>T
XM_017019364.2:c.-562G>T	XP_016874853.1:n.-562G>T
XM_017019366.2:c.-729G>T	XP_016874855.1:n.-729G>T
XM_017019367.2:c.-560G>T	XP_016874856.1:n.-560G>T
XR_001749352.2:n.187-6081C>A
XR_001749354.2:n.187-6081C>A
NM_002562.6:c.-49G>T MANE Select	NP_002553.3:n.-49G>T
NR_033948.2:n.47G>T
NR_033949.2:n.47G>T
NR_033950.2:n.47G>T
NR_033951.2:n.47G>T
NR_033952.2:n.47G>T
NR_033953.2:n.47G>T
NR_033954.2:n.47G>T
NR_033955.2:n.47G>T
NR_033956.2:n.47G>T