Canonical Allele Identifier: CA2348757223

Gene: PLCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.8134057A= , CM000682.2:g.8134057A=	GRCh38
NC_000020.10:g.8114704A= , CM000682.1:g.8114704A=	GRCh37
NC_000020.9:g.8062704A=	NCBI36
NG_028168.1:g.6409A=

Transcript Alleles

HGVS	Amino-acid Change
NM_015192.4:c.99+1307A= MANE Select	NP_056007.1:n.99+1307A=
ENST00000338037.11:c.99+1307A= MANE Select	ENSP00000338185.6:n.99+1307A=
NM_015192.3:c.99+1307A=	NP_056007.1:n.99+1307A=
NM_182734.2:c.99+1307A=	NP_877398.1:n.99+1307A=
NM_182734.3:c.99+1307A=	NP_877398.1:n.99+1307A=
ENST00000338037.10:c.99+1307A=	ENSP00000338185.6:n.99+1307A=
ENST00000378637.6:c.99+1307A=	ENSP00000367904.2:n.99+1307A=
ENST00000378641.7:c.99+1307A=	ENSP00000367908.3:n.99+1307A=
ENST00000404098.6:c.99+1307A=	ENSP00000384001.3:n.99+1307A=
ENST00000625874.2:c.-204-16237A=	ENSP00000486301.1:n.-204-16237A=
ENST00000626161.1:n.235+1307A=
ENST00000629992.2:c.99+1307A=	ENSP00000486531.1:n.99+1307A=
ENST00000630495.2:c.-282-7814A=	ENSP00000486655.1:n.-282-7814A=
ENST00000636319.1:c.99+1307A=	ENSP00000490455.1:n.99+1307A=
ENST00000637919.1:c.-204-16237A=	ENSP00000490862.1:n.-204-16237A=
XM_011529199.1:c.99+1307A=	XP_011527501.1:n.99+1307A=
XM_011529202.1:c.99+1307A=	XP_011527504.1:n.99+1307A=