Canonical Allele Identifier: CA509639158

Gene: PLCB1

Linked Data

• MyVariant Identifiers: chr20:g.8717755A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.8737108A>G , CM000682.2:g.8737108A>G	GRCh38
NC_000020.10:g.8717755A>G , CM000682.1:g.8717755A>G	GRCh37
NC_000020.9:g.8665755A>G	NCBI36
NG_028168.1:g.609460A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338037.11:c.2124A>G MANE Select	ENSP00000338185.6:p.Thr708=
ENST00000635830.1:n.2195A>G
ENST00000636825.1:n.1988A>G
ENST00000637919.1:c.1821A>G	ENSP00000490862.1:p.Thr607=
ENST00000338037.10:c.2124A>G	ENSP00000338185.6:p.Thr708=
ENST00000378637.6:c.2124A>G	ENSP00000367904.2:p.Thr708=
ENST00000378641.7:c.2124A>G	ENSP00000367908.3:p.Thr708=
ENST00000439627.2:c.81A>G	ENSP00000391162.1:p.Thr27=
ENST00000487210.5:c.1346A>G
ENST00000494924.2:n.1276A>G
ENST00000612075.4:c.1884A>G	ENSP00000479997.1:p.Thr628=
ENST00000617005.4:c.1884A>G	ENSP00000477664.1:p.Thr628=
ENST00000625874.2:c.1821A>G	ENSP00000486301.1:p.Thr607=
ENST00000626966.2:c.1821A>G	ENSP00000487075.1:p.Thr607=
NM_015192.3:c.2124A>G	NP_056007.1:p.Thr708=
NM_182734.2:c.2124A>G	NP_877398.1:p.Thr708=
XM_011529199.1:c.2124A>G	XP_011527501.1:p.Thr708=
XM_011529200.1:c.1908A>G	XP_011527502.1:p.Thr636=
XM_011529201.1:c.1821A>G	XP_011527503.1:p.Thr607=
XM_011529203.1:c.351A>G	XP_011527505.1:p.Thr117=
NM_015192.4:c.2124A>G MANE Select	NP_056007.1:p.Thr708=
NM_182734.3:c.2124A>G	NP_877398.1:p.Thr708=