Canonical Allele Identifier: CA2349020983

Gene: PLCB1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.8723905T>G , CM000682.2:g.8723905T>G	GRCh38
NC_000020.10:g.8704552T>G , CM000682.1:g.8704552T>G	GRCh37
NC_000020.9:g.8652552T>G	NCBI36
NG_028168.1:g.596257T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338037.11:c.1582-751T>G MANE Select	ENSP00000338185.6:n.1582-751T>G
ENST00000635830.1:n.1653-751T>G
ENST00000636319.1:c.*1025-751T>G	ENSP00000490455.1:n.*1025-751T>G
ENST00000636825.1:n.1446-751T>G
ENST00000637919.1:c.1279-751T>G	ENSP00000490862.1:n.1279-751T>G
ENST00000338037.10:c.1582-751T>G	ENSP00000338185.6:n.1582-751T>G
ENST00000378637.6:c.1582-751T>G	ENSP00000367904.2:n.1582-751T>G
ENST00000378641.7:c.1582-751T>G	ENSP00000367908.3:n.1582-751T>G
ENST00000487210.5:c.804-751T>G
ENST00000494924.2:n.734-751T>G
ENST00000612075.4:c.1342-751T>G	ENSP00000479997.1:n.1342-751T>G
ENST00000617005.4:c.1342-751T>G	ENSP00000477664.1:n.1342-751T>G
ENST00000625874.2:c.1279-751T>G	ENSP00000486301.1:n.1279-751T>G
ENST00000626966.2:c.1279-751T>G	ENSP00000487075.1:n.1279-751T>G
NM_015192.3:c.1582-751T>G	NP_056007.1:n.1582-751T>G
NM_182734.2:c.1582-751T>G	NP_877398.1:n.1582-751T>G
XM_011529199.1:c.1582-751T>G	XP_011527501.1:n.1582-751T>G
XM_011529200.1:c.1366-751T>G	XP_011527502.1:n.1366-751T>G
XM_011529201.1:c.1279-751T>G	XP_011527503.1:n.1279-751T>G
XM_011529202.1:c.1582-751T>G	XP_011527504.1:n.1582-751T>G
NM_015192.4:c.1582-751T>G MANE Select	NP_056007.1:n.1582-751T>G
NM_182734.3:c.1582-751T>G	NP_877398.1:n.1582-751T>G