Canonical Allele Identifier: CA2838296774

Gene: BCL3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44756418C>T , CM000681.2:g.44756418C>T	GRCh38
NC_000019.9:g.45259675C>T , CM000681.1:g.45259675C>T	GRCh37
NC_000019.8:g.49951515C>T	NCBI36
NG_052809.1:g.18798C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000164227.10:c.519+78C>T MANE Select	ENSP00000164227.5:n.519+78C>T
ENST00000164227.9:c.519+78C>T	ENSP00000164227.5:n.519+78C>T
ENST00000403534.7:n.687+78C>T
ENST00000444487.1:c.169+78C>T
ENST00000464319.1:n.196+78C>T
ENST00000473468.1:n.435+78C>T
NM_005178.4:c.519+78C>T	NP_005169.2:n.519+78C>T
XM_011527197.1:c.519+78C>T	XP_011525499.1:n.519+78C>T
XM_011527198.1:c.519+78C>T	XP_011525500.1:n.519+78C>T
XM_011527199.1:c.519+78C>T	XP_011525501.1:n.519+78C>T
XM_011527200.1:c.231+78C>T	XP_011525502.1:n.231+78C>T
XM_011527197.2:c.774+78C>T	XP_011525499.2:n.774+78C>T
XM_011527198.3:c.1185+78C>T	XP_011525500.2:n.1185+78C>T
XM_011527200.2:c.231+78C>T	XP_011525502.1:n.231+78C>T
XM_017027109.1:c.399+78C>T	XP_016882598.1:n.399+78C>T
XM_017027110.1:c.399+78C>T	XP_016882599.1:n.399+78C>T
NM_005178.5:c.519+78C>T MANE Select	NP_005169.2:n.519+78C>T