Canonical Allele Identifier: CA2067768065

Gene: P2RX7

Linked Data

• dbSNP Id: rs1872717006
• gnomAD v4: 12-121132886-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121132886C>T , CM000674.2:g.121132886C>T	GRCh38
NC_000012.11:g.121570689C>T , CM000674.1:g.121570689C>T	GRCh37
NC_000012.10:g.120055072C>T	NCBI36
NG_011471.2:g.5012C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.-85C>T MANE Select	ENSP00000330696.6:n.-85C>T
ENST00000328963.9:c.-85C>T	ENSP00000330696.6:n.-85C>T
ENST00000535928.5:c.-85C>T	ENSP00000439961.1:n.-85C>T
ENST00000537312.5:c.-85C>T	ENSP00000438586.1:n.-85C>T
NM_002562.5:c.-85C>T	NP_002553.3:n.-85C>T
NR_033948.1:n.59C>T
NR_033949.1:n.59C>T
NR_033950.1:n.59C>T
NR_033951.1:n.59C>T
NR_033952.1:n.59C>T
NR_033953.1:n.68C>T
NR_033954.1:n.59C>T
NR_033955.1:n.59C>T
NR_033956.1:n.59C>T
XM_011538418.1:c.-85C>T	XP_011536720.1:n.-85C>T
XM_011538419.1:c.-228C>T	XP_011536721.1:n.-228C>T
XM_011538419.3:c.-228C>T	XP_011536721.1:n.-228C>T
XM_017019364.2:c.-598C>T	XP_016874853.1:n.-598C>T
XM_017019367.2:c.-596C>T	XP_016874856.1:n.-596C>T
XR_001749352.2:n.187-6045G>A
XR_001749354.2:n.187-6045G>A
NM_002562.6:c.-85C>T MANE Select	NP_002553.3:n.-85C>T
NR_033948.2:n.11C>T
NR_033949.2:n.11C>T
NR_033950.2:n.11C>T
NR_033951.2:n.11C>T
NR_033952.2:n.11C>T
NR_033953.2:n.11C>T
NR_033954.2:n.11C>T
NR_033955.2:n.11C>T
NR_033956.2:n.11C>T