Canonical Allele Identifier: CA509639034

Gene: PLCB1

Linked Data

• MyVariant Identifiers: chr20:g.8717728A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.8737081A>C , CM000682.2:g.8737081A>C	GRCh38
NC_000020.10:g.8717728A>C , CM000682.1:g.8717728A>C	GRCh37
NC_000020.9:g.8665728A>C	NCBI36
NG_028168.1:g.609433A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338037.11:c.2097A>C MANE Select	ENSP00000338185.6:p.Val699=
ENST00000635830.1:n.2168A>C
ENST00000636825.1:n.1961A>C
ENST00000637919.1:c.1794A>C	ENSP00000490862.1:p.Val598=
ENST00000338037.10:c.2097A>C	ENSP00000338185.6:p.Val699=
ENST00000378637.6:c.2097A>C	ENSP00000367904.2:p.Val699=
ENST00000378641.7:c.2097A>C	ENSP00000367908.3:p.Val699=
ENST00000439627.2:c.54A>C	ENSP00000391162.1:p.Val18=
ENST00000487210.5:c.1319A>C
ENST00000494924.2:n.1249A>C
ENST00000612075.4:c.1857A>C	ENSP00000479997.1:p.Val619=
ENST00000617005.4:c.1857A>C	ENSP00000477664.1:p.Val619=
ENST00000625874.2:c.1794A>C	ENSP00000486301.1:p.Val598=
ENST00000626966.2:c.1794A>C	ENSP00000487075.1:p.Val598=
NM_015192.3:c.2097A>C	NP_056007.1:p.Val699=
NM_182734.2:c.2097A>C	NP_877398.1:p.Val699=
XM_011529199.1:c.2097A>C	XP_011527501.1:p.Val699=
XM_011529200.1:c.1881A>C	XP_011527502.1:p.Val627=
XM_011529201.1:c.1794A>C	XP_011527503.1:p.Val598=
XM_011529203.1:c.324A>C	XP_011527505.1:p.Val108=
NM_015192.4:c.2097A>C MANE Select	NP_056007.1:p.Val699=
NM_182734.3:c.2097A>C	NP_877398.1:p.Val699=