Canonical Allele Identifier: CA2348801419

Gene: PLCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.8233139G= , CM000682.2:g.8233139G=	GRCh38
NC_000020.10:g.8213786G= , CM000682.1:g.8213786G=	GRCh37
NC_000020.9:g.8161786G=	NCBI36
NG_028168.1:g.105491G=

Transcript Alleles

HGVS	Amino-acid Change
NM_015192.4:c.177+82768G= MANE Select	NP_056007.1:n.177+82768G=
ENST00000338037.11:c.177+82768G= MANE Select	ENSP00000338185.6:n.177+82768G=
NM_015192.3:c.177+82768G=	NP_056007.1:n.177+82768G=
NM_182734.2:c.177+82768G=	NP_877398.1:n.177+82768G=
NM_182734.3:c.177+82768G=	NP_877398.1:n.177+82768G=
ENST00000338037.10:c.177+82768G=	ENSP00000338185.6:n.177+82768G=
ENST00000378637.6:c.177+82768G=	ENSP00000367904.2:n.177+82768G=
ENST00000378641.7:c.177+82768G=	ENSP00000367908.3:n.177+82768G=
ENST00000404098.6:c.177+82768G=	ENSP00000384001.3:n.177+82768G=
ENST00000625874.2:c.-127+82768G=	ENSP00000486301.1:n.-127+82768G=
ENST00000626161.1:n.313+82768G=
ENST00000629992.2:c.177+82768G=	ENSP00000486531.1:n.177+82768G=
ENST00000630495.2:c.-127+82768G=	ENSP00000486655.1:n.-127+82768G=
ENST00000630757.1:n.72+82768G=
ENST00000636319.1:c.177+82768G=	ENSP00000490455.1:n.177+82768G=
ENST00000637204.1:c.59+82756G=
ENST00000637919.1:c.-127+82768G=	ENSP00000490862.1:n.-127+82768G=
XM_011529199.1:c.177+82768G=	XP_011527501.1:n.177+82768G=
XM_011529202.1:c.177+82768G=	XP_011527504.1:n.177+82768G=