Canonical Allele Identifier: CA11616289

Gene: BCL6

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.187738921T>G , CM000665.2:g.187738921T>G	GRCh38
NC_000003.11:g.187456709T>G , CM000665.1:g.187456709T>G	GRCh37
NC_000003.10:g.188939403T>G	NCBI36
NG_007149.1:g.11615A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406870.7:c.-49-4014A>C MANE Select	ENSP00000384371.2:n.-49-4014A>C
ENST00000406870.6:c.-49-4014A>C	ENSP00000384371.2:n.-49-4014A>C
ENST00000470319.1:n.64-4014A>C
ENST00000480458.5:n.29-4014A>C
ENST00000496823.1:n.51-1647A>C
ENST00000621333.4:c.-49-4014A>C	ENSP00000479784.1:n.-49-4014A>C
NM_001706.4:c.-49-4014A>C	NP_001697.2:n.-49-4014A>C
XM_005247694.2:c.-1374A>C	XP_005247751.1:n.-1374A>C
XM_011513062.1:c.-49-4014A>C	XP_011511364.1:n.-49-4014A>C
XM_005247694.4:c.-1374A>C	XP_005247751.1:n.-1374A>C
XM_011513062.3:c.-49-4014A>C	XP_011511364.1:n.-49-4014A>C
NM_001706.5:c.-49-4014A>C MANE Select	NP_001697.2:n.-49-4014A>C