Canonical Allele Identifier: CA509639136

Gene: PLCB1

Linked Data

• MyVariant Identifiers: chr20:g.8717749G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.8737102G>C , CM000682.2:g.8737102G>C	GRCh38
NC_000020.10:g.8717749G>C , CM000682.1:g.8717749G>C	GRCh37
NC_000020.9:g.8665749G>C	NCBI36
NG_028168.1:g.609454G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338037.11:c.2118G>C MANE Select	ENSP00000338185.6:p.Val706=
ENST00000635830.1:n.2189G>C
ENST00000636825.1:n.1982G>C
ENST00000637919.1:c.1815G>C	ENSP00000490862.1:p.Val605=
ENST00000338037.10:c.2118G>C	ENSP00000338185.6:p.Val706=
ENST00000378637.6:c.2118G>C	ENSP00000367904.2:p.Val706=
ENST00000378641.7:c.2118G>C	ENSP00000367908.3:p.Val706=
ENST00000439627.2:c.75G>C	ENSP00000391162.1:p.Val25=
ENST00000487210.5:c.1340G>C
ENST00000494924.2:n.1270G>C
ENST00000612075.4:c.1878G>C	ENSP00000479997.1:p.Val626=
ENST00000617005.4:c.1878G>C	ENSP00000477664.1:p.Val626=
ENST00000625874.2:c.1815G>C	ENSP00000486301.1:p.Val605=
ENST00000626966.2:c.1815G>C	ENSP00000487075.1:p.Val605=
NM_015192.3:c.2118G>C	NP_056007.1:p.Val706=
NM_182734.2:c.2118G>C	NP_877398.1:p.Val706=
XM_011529199.1:c.2118G>C	XP_011527501.1:p.Val706=
XM_011529200.1:c.1902G>C	XP_011527502.1:p.Val634=
XM_011529201.1:c.1815G>C	XP_011527503.1:p.Val605=
XM_011529203.1:c.345G>C	XP_011527505.1:p.Val115=
NM_015192.4:c.2118G>C MANE Select	NP_056007.1:p.Val706=
NM_182734.3:c.2118G>C	NP_877398.1:p.Val706=