Canonical Allele Identifier: CA509638984

Gene: PLCB1

Linked Data

• MyVariant Identifiers: chr20:g.8717716T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.8737069T>C , CM000682.2:g.8737069T>C	GRCh38
NC_000020.10:g.8717716T>C , CM000682.1:g.8717716T>C	GRCh37
NC_000020.9:g.8665716T>C	NCBI36
NG_028168.1:g.609421T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338037.11:c.2085T>C MANE Select	ENSP00000338185.6:p.Thr695=
ENST00000635830.1:n.2156T>C
ENST00000636825.1:n.1949T>C
ENST00000637919.1:c.1782T>C	ENSP00000490862.1:p.Thr594=
ENST00000338037.10:c.2085T>C	ENSP00000338185.6:p.Thr695=
ENST00000378637.6:c.2085T>C	ENSP00000367904.2:p.Thr695=
ENST00000378641.7:c.2085T>C	ENSP00000367908.3:p.Thr695=
ENST00000439627.2:c.42T>C	ENSP00000391162.1:p.Thr14=
ENST00000487210.5:c.1307T>C
ENST00000494924.2:n.1237T>C
ENST00000612075.4:c.1845T>C	ENSP00000479997.1:p.Thr615=
ENST00000617005.4:c.1845T>C	ENSP00000477664.1:p.Thr615=
ENST00000625874.2:c.1782T>C	ENSP00000486301.1:p.Thr594=
ENST00000626966.2:c.1782T>C	ENSP00000487075.1:p.Thr594=
NM_015192.3:c.2085T>C	NP_056007.1:p.Thr695=
NM_182734.2:c.2085T>C	NP_877398.1:p.Thr695=
XM_011529199.1:c.2085T>C	XP_011527501.1:p.Thr695=
XM_011529200.1:c.1869T>C	XP_011527502.1:p.Thr623=
XM_011529201.1:c.1782T>C	XP_011527503.1:p.Thr594=
XM_011529203.1:c.312T>C	XP_011527505.1:p.Thr104=
NM_015192.4:c.2085T>C MANE Select	NP_056007.1:p.Thr695=
NM_182734.3:c.2085T>C	NP_877398.1:p.Thr695=