Canonical Allele Identifier: CA2349026960
Gene: PLCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.8737169G= , CM000682.2:g.8737169G= GRCh38
NC_000020.10:g.8717816G= , CM000682.1:g.8717816G= GRCh37
NC_000020.9:g.8665816G= NCBI36
NG_028168.1:g.609521G=

Transcript Alleles

HGVS Amino-acid change
ENST00000338037.11:c.2185G= MANE Select ENSP00000338185.6:p.Glu729=
ENST00000635830.1:n.2256G=
ENST00000636825.1:n.2049G=
ENST00000637919.1:c.1882G= ENSP00000490862.1:p.Glu628=
ENST00000338037.10:c.2185G= ENSP00000338185.6:p.Glu729=
ENST00000378637.6:c.2185G= ENSP00000367904.2:p.Glu729=
ENST00000378641.7:c.2185G= ENSP00000367908.3:p.Glu729=
ENST00000439627.2:c.142G= ENSP00000391162.1:p.Glu48=
ENST00000487210.5:c.1407G=
ENST00000494924.2:n.1337G=
ENST00000612075.4:c.1945G= ENSP00000479997.1:p.Glu649=
ENST00000617005.4:c.1945G= ENSP00000477664.1:p.Glu649=
ENST00000625874.2:c.1882G= ENSP00000486301.1:p.Glu628=
ENST00000626966.2:c.1882G= ENSP00000487075.1:p.Glu628=
NM_015192.3:c.2185G= NP_056007.1:p.Glu729=
NM_182734.2:c.2185G= NP_877398.1:p.Glu729=
XM_011529199.1:c.2185G= XP_011527501.1:p.Glu729=
XM_011529200.1:c.1969G= XP_011527502.1:p.Glu657=
XM_011529201.1:c.1882G= XP_011527503.1:p.Glu628=
XM_011529203.1:c.412G= XP_011527505.1:p.Glu138=
NM_015192.4:c.2185G= MANE Select NP_056007.1:p.Glu729=
NM_182734.3:c.2185G= NP_877398.1:p.Glu729=