Canonical Allele Identifier: CA684502113

Gene: P2RX4

Linked Data

• dbSNP Id: rs1242685589
• gnomAD v4: 12-121222044-T-C
• MyVariant Identifiers: chr12:g.121659847T>C (hg19) ; chr12:g.121222044T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121222044T>C , CM000674.2:g.121222044T>C	GRCh38
NC_000012.11:g.121659847T>C , CM000674.1:g.121659847T>C	GRCh37
NC_000012.10:g.120144230T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000337233.9:c.355-50T>C MANE Select	ENSP00000336607.4:n.355-50T>C
ENST00000314442.7:n.4489-50T>C
ENST00000337233.8:c.355-50T>C	ENSP00000336607.4:n.355-50T>C
ENST00000359949.11:c.403-50T>C	ENSP00000353032.7:n.403-50T>C
ENST00000499638.6:n.391-50T>C
ENST00000538417.2:c.285-50T>C
ENST00000538701.5:c.135-6489T>C	ENSP00000444033.1:n.135-6489T>C
ENST00000540930.5:n.391-50T>C
ENST00000541187.5:n.201-50T>C
ENST00000542067.5:c.355-50T>C	ENSP00000438329.1:n.355-50T>C
ENST00000543171.5:c.355-50T>C	ENSP00000438131.2:n.355-50T>C
ENST00000543318.5:c.355-50T>C	ENSP00000444274.1:n.355-50T>C
ENST00000543430.5:n.403-50T>C
ENST00000543984.5:c.*48-50T>C	ENSP00000439386.1:n.*48-50T>C
NM_001256796.1:c.403-50T>C	NP_001243725.1:n.403-50T>C
NM_001261397.1:c.355-50T>C	NP_001248326.1:n.355-50T>C
NM_001261398.1:c.355-50T>C	NP_001248327.1:n.355-50T>C
NM_002560.2:c.355-50T>C	NP_002551.2:n.355-50T>C
NR_046372.1:n.659-50T>C
NR_046373.1:n.511-50T>C
XM_011538416.1:c.135-6489T>C	XP_011536718.1:n.135-6489T>C
XM_011538417.1:c.403-50T>C	XP_011536719.1:n.403-50T>C
XR_944559.1:n.463-50T>C
XM_011538416.2:c.135-6489T>C	XP_011536718.1:n.135-6489T>C
XR_001748726.2:n.409-50T>C
XR_001748727.1:n.472-50T>C
XR_001748728.1:n.472-50T>C
XR_001748729.2:n.409-50T>C
XR_944559.2:n.462-50T>C
NM_001256796.2:c.403-50T>C	NP_001243725.1:n.403-50T>C
NM_001261397.2:c.355-50T>C	NP_001248326.1:n.355-50T>C
NM_001261398.2:c.355-50T>C	NP_001248327.1:n.355-50T>C
NM_002560.3:c.355-50T>C MANE Select	NP_002551.2:n.355-50T>C
NR_046372.2:n.391-50T>C
NR_046373.2:n.243-50T>C