Canonical Allele Identifier: CA154258

Gene: PLCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.8150296C>T , CM000682.2:g.8150296C>T	GRCh38
NC_000020.10:g.8130943C>T , CM000682.1:g.8130943C>T	GRCh37
NC_000020.9:g.8078943C>T	NCBI36
NG_028168.1:g.22648C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338037.11:c.102C>T MANE Select	ENSP00000338185.6:p.Asp34=
ENST00000636319.1:c.102C>T	ENSP00000490455.1:p.Asp34=
ENST00000637919.1:c.-202C>T	ENSP00000490862.1:n.-202C>T
ENST00000338037.10:c.102C>T	ENSP00000338185.6:p.Asp34=
ENST00000378637.6:c.102C>T	ENSP00000367904.2:p.Asp34=
ENST00000378641.7:c.102C>T	ENSP00000367908.3:p.Asp34=
ENST00000404098.6:c.102C>T	ENSP00000384001.3:p.Asp34=
ENST00000625874.2:c.-202C>T	ENSP00000486301.1:n.-202C>T
ENST00000626161.1:n.238C>T
ENST00000629992.2:c.102C>T	ENSP00000486531.1:p.Asp34=
ENST00000630495.2:c.-202C>T	ENSP00000486655.1:n.-202C>T
NM_015192.3:c.102C>T	NP_056007.1:p.Asp34=
NM_182734.2:c.102C>T	NP_877398.1:p.Asp34=
XM_011529199.1:c.102C>T	XP_011527501.1:p.Asp34=
XM_011529202.1:c.102C>T	XP_011527504.1:p.Asp34=
NM_015192.4:c.102C>T MANE Select	NP_056007.1:p.Asp34=
NM_182734.3:c.102C>T	NP_877398.1:p.Asp34=