Canonical Allele Identifier: CA2308718921

Gene: BCL2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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