Canonical Allele Identifier: CA2308718905

Gene: BCL2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318757C= , CM000680.2:g.63318757C=	GRCh38
NC_000018.9:g.60985990C= , CM000680.1:g.60985990C=	GRCh37
NC_000018.8:g.59136970C=	NCBI36
NG_009361.1:g.5624G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-91G= MANE Select	ENSP00000329623.3:n.-91G=
ENST00000333681.4:c.-91G=	ENSP00000329623.3:n.-91G=
ENST00000398117.1:c.-91G=	ENSP00000381185.1:n.-91G=
ENST00000589955.2:c.-91G=	ENSP00000466417.1:n.-91G=
NM_000633.2:c.-91G=	NP_000624.2:n.-91G=
NM_000657.2:c.-91G=	NP_000648.2:n.-91G=
XM_011526135.1:c.-91G=	XP_011524437.1:n.-91G=
XR_935246.1:n.1022G=
XR_935247.1:n.1022G=
XR_935248.1:n.801G=
XM_011526135.3:c.-91G=	XP_011524437.1:n.-91G=
XM_017025917.2:c.-91G=	XP_016881406.1:n.-91G=
XR_935248.3:n.1303G=
NM_000633.3:c.-91G= MANE Select	NP_000624.2:n.-91G=
NM_000657.3:c.-91G=	NP_000648.2:n.-91G=