Canonical Allele Identifier: CA244569173

Gene: P2RX4

Linked Data

• dbSNP Id: rs77300956
• gnomAD v4: 12-121232385-T-C
• MyVariant Identifiers: chr12:g.121670188T>C (hg19) ; chr12:g.121232385T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121232385T>C , CM000674.2:g.121232385T>C	GRCh38
NC_000012.11:g.121670188T>C , CM000674.1:g.121670188T>C	GRCh37
NC_000012.10:g.120154571T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000337233.9:c.885-29T>C MANE Select	ENSP00000336607.4:n.885-29T>C
ENST00000337233.8:c.885-29T>C	ENSP00000336607.4:n.885-29T>C
ENST00000359949.11:c.933-29T>C	ENSP00000353032.7:n.933-29T>C
ENST00000499638.6:n.1878-29T>C
ENST00000538417.2:c.743T>C
ENST00000541187.5:n.730-29T>C
ENST00000542067.5:c.804-29T>C	ENSP00000438329.1:n.804-29T>C
ENST00000543171.5:c.885-29T>C	ENSP00000438131.2:n.885-29T>C
ENST00000543318.5:c.*476-29T>C	ENSP00000444274.1:n.*476-29T>C
ENST00000543430.5:n.836-29T>C
ENST00000543984.5:c.*578-29T>C	ENSP00000439386.1:n.*578-29T>C
NM_001256796.1:c.933-29T>C	NP_001243725.1:n.933-29T>C
NM_001261397.1:c.804-29T>C	NP_001248326.1:n.804-29T>C
NM_001261398.1:c.885-29T>C	NP_001248327.1:n.885-29T>C
NM_002560.2:c.885-29T>C	NP_002551.2:n.885-29T>C
NR_046372.1:n.1227-29T>C
NR_046373.1:n.1041-29T>C
XM_011538416.1:c.495-29T>C	XP_011536718.1:n.495-29T>C
XR_944559.1:n.922-29T>C
XM_011538416.2:c.495-29T>C	XP_011536718.1:n.495-29T>C
XR_001748726.2:n.868-29T>C
XR_001748727.1:n.1017-29T>C
XR_001748728.1:n.946-29T>C
XR_001748729.2:n.954-29T>C
XR_944559.2:n.921-29T>C
NM_001256796.2:c.933-29T>C	NP_001243725.1:n.933-29T>C
NM_001261397.2:c.804-29T>C	NP_001248326.1:n.804-29T>C
NM_001261398.2:c.885-29T>C	NP_001248327.1:n.885-29T>C
NM_002560.3:c.885-29T>C MANE Select	NP_002551.2:n.885-29T>C
NR_046372.2:n.959-29T>C
NR_046373.2:n.773-29T>C