Canonical Allele Identifier: CA2308718979

Gene: BCL2

Linked Data

• dbSNP Id: rs1913604588
• gnomAD v4: 18-63318932-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318933del , CM000680.2:g.63318933del	GRCh38
NC_000018.9:g.60986166del , CM000680.1:g.60986166del	GRCh37
NC_000018.8:g.59137146del	NCBI36
NG_009361.1:g.5448del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-267del MANE Select	ENSP00000329623.3:n.-267del
ENST00000333681.4:c.-267del	ENSP00000329623.3:n.-267del
ENST00000398117.1:c.-267del	ENSP00000381185.1:n.-267del
NM_000633.2:c.-267del	NP_000624.2:n.-267del
NM_000657.2:c.-267del	NP_000648.2:n.-267del
XM_011526135.1:c.-267del	XP_011524437.1:n.-267del
XR_935246.1:n.846del
XR_935247.1:n.846del
XR_935248.1:n.625del
XM_011526135.3:c.-267del	XP_011524437.1:n.-267del
XM_017025917.2:c.-267del	XP_016881406.1:n.-267del
XR_935248.3:n.1127del
NM_000633.3:c.-267del MANE Select	NP_000624.2:n.-267del
NM_000657.3:c.-267del	NP_000648.2:n.-267del