Canonical Allele Identifier: CA607882471

Gene: P2RX7

Linked Data

• dbSNP Id: rs1401998499
• gnomAD v2: 12-121570765-G-T
• MyVariant Identifiers: chr12:g.121570765G>T (hg19) ; chr12:g.121132962G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121132962G>T , CM000674.2:g.121132962G>T	GRCh38
NC_000012.11:g.121570765G>T , CM000674.1:g.121570765G>T	GRCh37
NC_000012.10:g.120055148G>T	NCBI36
NG_011471.2:g.5088G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.-9G>T MANE Select	ENSP00000330696.6:n.-9G>T
ENST00000261826.10:c.-9G>T	ENSP00000261826.6:n.-9G>T
ENST00000328963.9:c.-9G>T	ENSP00000330696.6:n.-9G>T
ENST00000535928.5:c.-9G>T	ENSP00000439961.1:n.-9G>T
ENST00000537312.5:c.-9G>T	ENSP00000438586.1:n.-9G>T
ENST00000539695.5:n.61G>T
ENST00000545434.5:c.-9G>T	ENSP00000445564.1:n.-9G>T
NM_002562.5:c.-9G>T	NP_002553.3:n.-9G>T
NR_033948.1:n.135G>T
NR_033949.1:n.135G>T
NR_033950.1:n.135G>T
NR_033951.1:n.135G>T
NR_033952.1:n.135G>T
NR_033953.1:n.144G>T
NR_033954.1:n.135G>T
NR_033955.1:n.135G>T
NR_033956.1:n.135G>T
XM_011538418.1:c.-9G>T	XP_011536720.1:n.-9G>T
XM_011538419.1:c.-152G>T	XP_011536721.1:n.-152G>T
XM_011538419.3:c.-152G>T	XP_011536721.1:n.-152G>T
XM_017019364.2:c.-522G>T	XP_016874853.1:n.-522G>T
XM_017019365.2:c.-353G>T	XP_016874854.1:n.-353G>T
XM_017019366.2:c.-689G>T	XP_016874855.1:n.-689G>T
XM_017019367.2:c.-520G>T	XP_016874856.1:n.-520G>T
XR_001749352.2:n.187-6121C>A
XR_001749354.2:n.187-6121C>A
NM_002562.6:c.-9G>T MANE Select	NP_002553.3:n.-9G>T
NR_033948.2:n.87G>T
NR_033949.2:n.87G>T
NR_033950.2:n.87G>T
NR_033951.2:n.87G>T
NR_033952.2:n.87G>T
NR_033953.2:n.87G>T
NR_033954.2:n.87G>T
NR_033955.2:n.87G>T
NR_033956.2:n.87G>T