Canonical Allele Identifier: CA2750799

Gene: BCL6

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.187729778G>A , CM000665.2:g.187729778G>A	GRCh38
NC_000003.11:g.187447566G>A , CM000665.1:g.187447566G>A	GRCh37
NC_000003.10:g.188930260G>A	NCBI36
NG_007149.1:g.20758C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001706.5:c.627C>T MANE Select	NP_001697.2:p.Ser209=
ENST00000406870.7:c.627C>T MANE Select	ENSP00000384371.2:p.Ser209=
NM_001130845.1:c.627C>T	NP_001124317.1:p.Ser209=
NM_001130845.2:c.627C>T	NP_001124317.1:p.Ser209=
NM_001134738.1:c.627C>T	NP_001128210.1:p.Ser209=
NM_001706.4:c.627C>T	NP_001697.2:p.Ser209=
NR_034062.1:n.294-2593G>A
ENST00000232014.8:c.627C>T	ENSP00000232014.4:p.Ser209=
ENST00000406870.6:c.627C>T	ENSP00000384371.2:p.Ser209=
ENST00000419510.6:c.*397C>T	ENSP00000398014.2:n.*397C>T
ENST00000450123.6:c.627C>T	ENSP00000413122.2:p.Ser209=
ENST00000621333.4:c.627C>T	ENSP00000479784.1:p.Ser209=
XM_005247694.2:c.627C>T	XP_005247751.1:p.Ser209=
XM_005247694.4:c.627C>T	XP_005247751.1:p.Ser209=
XM_011513062.1:c.627C>T	XP_011511364.1:p.Ser209=
XM_011513062.3:c.627C>T	XP_011511364.1:p.Ser209=