Canonical Allele Identifier: CA2308713150

Gene: BCL2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63305155G= , CM000680.2:g.63305155G=	GRCh38
NC_000018.9:g.60972388G= , CM000680.1:g.60972388G=	GRCh37
NC_000018.8:g.59123368G=	NCBI36
NG_009361.1:g.19226C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000333681.5:c.585+12927C= MANE Select	ENSP00000329623.3:n.585+12927C=
ENST00000677227.1:c.585+12927C=	ENSP00000504566.1:n.585+12927C=
ENST00000678134.1:c.586-3290C=	ENSP00000503628.1:n.586-3290C=
ENST00000678349.1:c.1137+12375C=	ENSP00000504190.1:n.1137+12375C=
ENST00000333681.4:c.585+12927C=	ENSP00000329623.3:n.585+12927C=
ENST00000398117.1:c.585+12927C=	ENSP00000381185.1:n.585+12927C=
NM_000633.2:c.585+12927C=	NP_000624.2:n.585+12927C=
XM_011526135.1:c.586-2308C=	XP_011524437.1:n.586-2308C=
XR_935246.1:n.1697+12927C=
XR_935247.1:n.1697+12927C=
XR_935248.1:n.1476+12927C=
XM_011526135.3:c.586-2308C=	XP_011524437.1:n.586-2308C=
XM_017025917.2:c.586-3290C=	XP_016881406.1:n.586-3290C=
XR_935248.3:n.1978+12927C=
NM_000633.3:c.585+12927C= MANE Select	NP_000624.2:n.585+12927C=