Canonical Allele Identifier: CA2750653

Gene: BCL6

Linked Data

• ClinVar Variation Id: 781975
• ClinVar RCV Id: RCV000963295
• dbSNP Id: rs113668878
• ExAC: 3:187446335 A / G
• gnomAD v2: 3-187446335-A-G
• gnomAD v3: 3-187728547-A-G
• gnomAD v4: 3-187728547-A-G
• MyVariant Identifiers: chr3:g.187446335A>G (hg19) ; chr3:g.187728547A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.187728547A>G , CM000665.2:g.187728547A>G	GRCh38
NC_000003.11:g.187446335A>G , CM000665.1:g.187446335A>G	GRCh37
NC_000003.10:g.188929029A>G	NCBI36
NG_007149.1:g.21989T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406870.7:c.1356-3T>C MANE Select	ENSP00000384371.2:n.1356-3T>C
ENST00000232014.8:c.1356-3T>C	ENSP00000232014.4:n.1356-3T>C
ENST00000406870.6:c.1356-3T>C	ENSP00000384371.2:n.1356-3T>C
ENST00000419510.6:c.*1126-3T>C	ENSP00000398014.2:n.*1126-3T>C
ENST00000450123.6:c.1356-3T>C	ENSP00000413122.2:n.1356-3T>C
ENST00000621333.4:c.1356-3T>C	ENSP00000479784.1:n.1356-3T>C
NM_001130845.1:c.1356-3T>C	NP_001124317.1:n.1356-3T>C
NM_001134738.1:c.1356-3T>C	NP_001128210.1:n.1356-3T>C
NM_001706.4:c.1356-3T>C	NP_001697.2:n.1356-3T>C
NR_034062.1:n.294-3824A>G
XM_005247694.2:c.1356-3T>C	XP_005247751.1:n.1356-3T>C
XM_011513062.1:c.1356-3T>C	XP_011511364.1:n.1356-3T>C
XM_005247694.4:c.1356-3T>C	XP_005247751.1:n.1356-3T>C
XM_011513062.3:c.1356-3T>C	XP_011511364.1:n.1356-3T>C
NM_001706.5:c.1356-3T>C MANE Select	NP_001697.2:n.1356-3T>C
NM_001130845.2:c.1356-3T>C	NP_001124317.1:n.1356-3T>C