Canonical Allele Identifier: CA408206597

Gene: PLCB1

Linked Data

• MyVariant Identifiers: chr20:g.8717714A>G (hg19) ; chr20:g.8737067A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.8737067A>G , CM000682.2:g.8737067A>G	GRCh38
NC_000020.10:g.8717714A>G , CM000682.1:g.8717714A>G	GRCh37
NC_000020.9:g.8665714A>G	NCBI36
NG_028168.1:g.609419A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338037.11:c.2083A>G MANE Select	ENSP00000338185.6:p.Thr695Ala
ENST00000635830.1:n.2154A>G
ENST00000636825.1:n.1947A>G
ENST00000637919.1:c.1780A>G	ENSP00000490862.1:p.Thr594Ala
ENST00000338037.10:c.2083A>G	ENSP00000338185.6:p.Thr695Ala
ENST00000378637.6:c.2083A>G	ENSP00000367904.2:p.Thr695Ala
ENST00000378641.7:c.2083A>G	ENSP00000367908.3:p.Thr695Ala
ENST00000439627.2:c.40A>G	ENSP00000391162.1:p.Thr14Ala
ENST00000487210.5:c.1305A>G
ENST00000494924.2:n.1235A>G
ENST00000612075.4:c.1843A>G	ENSP00000479997.1:p.Thr615Ala
ENST00000617005.4:c.1843A>G	ENSP00000477664.1:p.Thr615Ala
ENST00000625874.2:c.1780A>G	ENSP00000486301.1:p.Thr594Ala
ENST00000626966.2:c.1780A>G	ENSP00000487075.1:p.Thr594Ala
NM_015192.3:c.2083A>G	NP_056007.1:p.Thr695Ala
NM_182734.2:c.2083A>G	NP_877398.1:p.Thr695Ala
XM_011529199.1:c.2083A>G	XP_011527501.1:p.Thr695Ala
XM_011529200.1:c.1867A>G	XP_011527502.1:p.Thr623Ala
XM_011529201.1:c.1780A>G	XP_011527503.1:p.Thr594Ala
XM_011529203.1:c.310A>G	XP_011527505.1:p.Thr104Ala
NM_015192.4:c.2083A>G MANE Select	NP_056007.1:p.Thr695Ala
NM_182734.3:c.2083A>G	NP_877398.1:p.Thr695Ala