Canonical Allele Identifier: CA2621395759

Gene: P2RX7

Linked Data

• gnomAD v4: 12-121132938-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121132938G>C , CM000674.2:g.121132938G>C	GRCh38
NC_000012.11:g.121570741G>C , CM000674.1:g.121570741G>C	GRCh37
NC_000012.10:g.120055124G>C	NCBI36
NG_011471.2:g.5064G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.-33G>C MANE Select	ENSP00000330696.6:n.-33G>C
ENST00000261826.10:c.-33G>C	ENSP00000261826.6:n.-33G>C
ENST00000328963.9:c.-33G>C	ENSP00000330696.6:n.-33G>C
ENST00000535928.5:c.-33G>C	ENSP00000439961.1:n.-33G>C
ENST00000537312.5:c.-33G>C	ENSP00000438586.1:n.-33G>C
ENST00000539695.5:n.37G>C
ENST00000545434.5:c.-33G>C	ENSP00000445564.1:n.-33G>C
NM_002562.5:c.-33G>C	NP_002553.3:n.-33G>C
NR_033948.1:n.111G>C
NR_033949.1:n.111G>C
NR_033950.1:n.111G>C
NR_033951.1:n.111G>C
NR_033952.1:n.111G>C
NR_033953.1:n.120G>C
NR_033954.1:n.111G>C
NR_033955.1:n.111G>C
NR_033956.1:n.111G>C
XM_011538418.1:c.-33G>C	XP_011536720.1:n.-33G>C
XM_011538419.1:c.-176G>C	XP_011536721.1:n.-176G>C
XM_011538419.3:c.-176G>C	XP_011536721.1:n.-176G>C
XM_017019364.2:c.-546G>C	XP_016874853.1:n.-546G>C
XM_017019365.2:c.-377G>C	XP_016874854.1:n.-377G>C
XM_017019366.2:c.-713G>C	XP_016874855.1:n.-713G>C
XM_017019367.2:c.-544G>C	XP_016874856.1:n.-544G>C
XR_001749352.2:n.187-6097C>G
XR_001749354.2:n.187-6097C>G
NM_002562.6:c.-33G>C MANE Select	NP_002553.3:n.-33G>C
NR_033948.2:n.63G>C
NR_033949.2:n.63G>C
NR_033950.2:n.63G>C
NR_033951.2:n.63G>C
NR_033952.2:n.63G>C
NR_033953.2:n.63G>C
NR_033954.2:n.63G>C
NR_033955.2:n.63G>C
NR_033956.2:n.63G>C