Canonical Allele Identifier: CA991105581

Gene: BCL2

Linked Data

• dbSNP Id: rs1913597680
• gnomAD v3: 18-63318795-A-AG
• gnomAD v4: 18-63318795-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318800dup , CM000680.2:g.63318800dup	GRCh38
NC_000018.9:g.60986033dup , CM000680.1:g.60986033dup	GRCh37
NC_000018.8:g.59137013dup	NCBI36
NG_009361.1:g.5585dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-130dup MANE Select	ENSP00000329623.3:n.-130dup
ENST00000333681.4:c.-130dup	ENSP00000329623.3:n.-130dup
ENST00000398117.1:c.-130dup	ENSP00000381185.1:n.-130dup
ENST00000589955.2:c.-130dup	ENSP00000466417.1:n.-130dup
NM_000633.2:c.-130dup	NP_000624.2:n.-130dup
NM_000657.2:c.-130dup	NP_000648.2:n.-130dup
XM_011526135.1:c.-130dup	XP_011524437.1:n.-130dup
XR_935246.1:n.983dup
XR_935247.1:n.983dup
XR_935248.1:n.762dup
XM_011526135.3:c.-130dup	XP_011524437.1:n.-130dup
XM_017025917.2:c.-130dup	XP_016881406.1:n.-130dup
XR_935248.3:n.1264dup
NM_000633.3:c.-130dup MANE Select	NP_000624.2:n.-130dup
NM_000657.3:c.-130dup	NP_000648.2:n.-130dup