Canonical Allele Identifier: CA2308718854

Gene: BCL2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318646T= , CM000680.2:g.63318646T=	GRCh38
NC_000018.9:g.60985879T= , CM000680.1:g.60985879T=	GRCh37
NC_000018.8:g.59136859T=	NCBI36
NG_009361.1:g.5735A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000333681.5:c.21A= MANE Select	ENSP00000329623.3:p.Thr7=
ENST00000677227.1:c.21A=	ENSP00000504566.1:p.Thr7=
ENST00000678134.1:c.21A=	ENSP00000503628.1:p.Thr7=
ENST00000678349.1:c.21A=	ENSP00000504190.1:p.Thr7=
ENST00000333681.4:c.21A=	ENSP00000329623.3:p.Thr7=
ENST00000398117.1:c.21A=	ENSP00000381185.1:p.Thr7=
ENST00000589955.2:c.21A=	ENSP00000466417.1:p.Thr7=
NM_000633.2:c.21A=	NP_000624.2:p.Thr7=
NM_000657.2:c.21A=	NP_000648.2:p.Thr7=
XM_011526135.1:c.21A=	XP_011524437.1:p.Thr7=
XR_935246.1:n.1133A=
XR_935247.1:n.1133A=
XR_935248.1:n.912A=
XM_011526135.3:c.21A=	XP_011524437.1:p.Thr7=
XM_017025917.2:c.21A=	XP_016881406.1:p.Thr7=
XR_935248.3:n.1414A=
NM_000633.3:c.21A= MANE Select	NP_000624.2:p.Thr7=
NM_000657.3:c.21A=	NP_000648.2:p.Thr7=