Canonical Allele Identifier: CA2067768438

Gene: P2RX7

Linked Data

• dbSNP Id: rs1872729623

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121132955G>C , CM000674.2:g.121132955G>C	GRCh38
NC_000012.11:g.121570758G>C , CM000674.1:g.121570758G>C	GRCh37
NC_000012.10:g.120055141G>C	NCBI36
NG_011471.2:g.5081G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.-16G>C MANE Select	ENSP00000330696.6:n.-16G>C
ENST00000261826.10:c.-16G>C	ENSP00000261826.6:n.-16G>C
ENST00000328963.9:c.-16G>C	ENSP00000330696.6:n.-16G>C
ENST00000535928.5:c.-16G>C	ENSP00000439961.1:n.-16G>C
ENST00000537312.5:c.-16G>C	ENSP00000438586.1:n.-16G>C
ENST00000539695.5:n.54G>C
ENST00000545434.5:c.-16G>C	ENSP00000445564.1:n.-16G>C
NM_002562.5:c.-16G>C	NP_002553.3:n.-16G>C
NR_033948.1:n.128G>C
NR_033949.1:n.128G>C
NR_033950.1:n.128G>C
NR_033951.1:n.128G>C
NR_033952.1:n.128G>C
NR_033953.1:n.137G>C
NR_033954.1:n.128G>C
NR_033955.1:n.128G>C
NR_033956.1:n.128G>C
XM_011538418.1:c.-16G>C	XP_011536720.1:n.-16G>C
XM_011538419.1:c.-159G>C	XP_011536721.1:n.-159G>C
XM_011538419.3:c.-159G>C	XP_011536721.1:n.-159G>C
XM_017019364.2:c.-529G>C	XP_016874853.1:n.-529G>C
XM_017019365.2:c.-360G>C	XP_016874854.1:n.-360G>C
XM_017019366.2:c.-696G>C	XP_016874855.1:n.-696G>C
XM_017019367.2:c.-527G>C	XP_016874856.1:n.-527G>C
XR_001749352.2:n.187-6114C>G
XR_001749354.2:n.187-6114C>G
NM_002562.6:c.-16G>C MANE Select	NP_002553.3:n.-16G>C
NR_033948.2:n.80G>C
NR_033949.2:n.80G>C
NR_033950.2:n.80G>C
NR_033951.2:n.80G>C
NR_033952.2:n.80G>C
NR_033953.2:n.80G>C
NR_033954.2:n.80G>C
NR_033955.2:n.80G>C
NR_033956.2:n.80G>C