Canonical Allele Identifier: CA607882461

Gene: P2RX7

Linked Data

• dbSNP Id: rs1478796608
• gnomAD v2: 12-121570723-A-T
• gnomAD v3: 12-121132920-A-T
• gnomAD v4: 12-121132920-A-T
• MyVariant Identifiers: chr12:g.121570723A>T (hg19) ; chr12:g.121132920A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121132920A>T , CM000674.2:g.121132920A>T	GRCh38
NC_000012.11:g.121570723A>T , CM000674.1:g.121570723A>T	GRCh37
NC_000012.10:g.120055106A>T	NCBI36
NG_011471.2:g.5046A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.-51A>T MANE Select	ENSP00000330696.6:n.-51A>T
ENST00000328963.9:c.-51A>T	ENSP00000330696.6:n.-51A>T
ENST00000535928.5:c.-51A>T	ENSP00000439961.1:n.-51A>T
ENST00000537312.5:c.-51A>T	ENSP00000438586.1:n.-51A>T
ENST00000539695.5:n.19A>T
NM_002562.5:c.-51A>T	NP_002553.3:n.-51A>T
NR_033948.1:n.93A>T
NR_033949.1:n.93A>T
NR_033950.1:n.93A>T
NR_033951.1:n.93A>T
NR_033952.1:n.93A>T
NR_033953.1:n.102A>T
NR_033954.1:n.93A>T
NR_033955.1:n.93A>T
NR_033956.1:n.93A>T
XM_011538418.1:c.-51A>T	XP_011536720.1:n.-51A>T
XM_011538419.1:c.-194A>T	XP_011536721.1:n.-194A>T
XM_011538419.3:c.-194A>T	XP_011536721.1:n.-194A>T
XM_017019364.2:c.-564A>T	XP_016874853.1:n.-564A>T
XM_017019366.2:c.-731A>T	XP_016874855.1:n.-731A>T
XM_017019367.2:c.-562A>T	XP_016874856.1:n.-562A>T
XR_001749352.2:n.187-6079T>A
XR_001749354.2:n.187-6079T>A
NM_002562.6:c.-51A>T MANE Select	NP_002553.3:n.-51A>T
NR_033948.2:n.45A>T
NR_033949.2:n.45A>T
NR_033950.2:n.45A>T
NR_033951.2:n.45A>T
NR_033952.2:n.45A>T
NR_033953.2:n.45A>T
NR_033954.2:n.45A>T
NR_033955.2:n.45A>T
NR_033956.2:n.45A>T