Canonical Allele Identifier: CA402633286

Gene: BCL2

Linked Data

• COSMIC: COSM4170963 ; COSM4170964 ; COSM4170965
• MyVariant Identifiers: chr18:g.60985884T>C (hg19) ; chr18:g.63318651T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318651T>C , CM000680.2:g.63318651T>C	GRCh38
NC_000018.9:g.60985884T>C , CM000680.1:g.60985884T>C	GRCh37
NC_000018.8:g.59136864T>C	NCBI36
NG_009361.1:g.5730A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000333681.5:c.16A>G MANE Select	ENSP00000329623.3:p.Arg6Gly
ENST00000677227.1:c.16A>G	ENSP00000504566.1:p.Arg6Gly
ENST00000678134.1:c.16A>G	ENSP00000503628.1:p.Arg6Gly
ENST00000678349.1:c.16A>G	ENSP00000504190.1:p.Arg6Gly
ENST00000333681.4:c.16A>G	ENSP00000329623.3:p.Arg6Gly
ENST00000398117.1:c.16A>G	ENSP00000381185.1:p.Arg6Gly
ENST00000589955.2:c.16A>G	ENSP00000466417.1:p.Arg6Gly
NM_000633.2:c.16A>G	NP_000624.2:p.Arg6Gly
NM_000657.2:c.16A>G	NP_000648.2:p.Arg6Gly
XM_011526135.1:c.16A>G	XP_011524437.1:p.Arg6Gly
XR_935246.1:n.1128A>G
XR_935247.1:n.1128A>G
XR_935248.1:n.907A>G
XM_011526135.3:c.16A>G	XP_011524437.1:p.Arg6Gly
XM_017025917.2:c.16A>G	XP_016881406.1:p.Arg6Gly
XR_935248.3:n.1409A>G
NM_000633.3:c.16A>G MANE Select	NP_000624.2:p.Arg6Gly
NM_000657.3:c.16A>G	NP_000648.2:p.Arg6Gly