Canonical Allele Identifier: CA2349026943

Gene: PLCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.8737073G= , CM000682.2:g.8737073G=	GRCh38
NC_000020.10:g.8717720G= , CM000682.1:g.8717720G=	GRCh37
NC_000020.9:g.8665720G=	NCBI36
NG_028168.1:g.609425G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338037.11:c.2089G= MANE Select	ENSP00000338185.6:p.Val697=
ENST00000635830.1:n.2160G=
ENST00000636825.1:n.1953G=
ENST00000637919.1:c.1786G=	ENSP00000490862.1:p.Val596=
ENST00000338037.10:c.2089G=	ENSP00000338185.6:p.Val697=
ENST00000378637.6:c.2089G=	ENSP00000367904.2:p.Val697=
ENST00000378641.7:c.2089G=	ENSP00000367908.3:p.Val697=
ENST00000439627.2:c.46G=	ENSP00000391162.1:p.Val16=
ENST00000487210.5:c.1311G=
ENST00000494924.2:n.1241G=
ENST00000612075.4:c.1849G=	ENSP00000479997.1:p.Val617=
ENST00000617005.4:c.1849G=	ENSP00000477664.1:p.Val617=
ENST00000625874.2:c.1786G=	ENSP00000486301.1:p.Val596=
ENST00000626966.2:c.1786G=	ENSP00000487075.1:p.Val596=
NM_015192.3:c.2089G=	NP_056007.1:p.Val697=
NM_182734.2:c.2089G=	NP_877398.1:p.Val697=
XM_011529199.1:c.2089G=	XP_011527501.1:p.Val697=
XM_011529200.1:c.1873G=	XP_011527502.1:p.Val625=
XM_011529201.1:c.1786G=	XP_011527503.1:p.Val596=
XM_011529203.1:c.316G=	XP_011527505.1:p.Val106=
NM_015192.4:c.2089G= MANE Select	NP_056007.1:p.Val697=
NM_182734.3:c.2089G=	NP_877398.1:p.Val697=