Canonical Allele Identifier: CA657487711

Gene: BCL2

Linked Data

• COSMIC: COSN4774906 ; COSN25215721 ; COSN25460812 ; COSN25468197 ; COSN25623824

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318672C>T , CM000680.2:g.63318672C>T	GRCh38
NC_000018.9:g.60985905C>T , CM000680.1:g.60985905C>T	GRCh37
NC_000018.8:g.59136885C>T	NCBI36
NG_009361.1:g.5709G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-6G>A MANE Select	ENSP00000329623.3:n.-6G>A
ENST00000333681.4:c.-6G>A	ENSP00000329623.3:n.-6G>A
ENST00000398117.1:c.-6G>A	ENSP00000381185.1:n.-6G>A
ENST00000589955.2:c.-6G>A	ENSP00000466417.1:n.-6G>A
NM_000633.2:c.-6G>A	NP_000624.2:n.-6G>A
NM_000657.2:c.-6G>A	NP_000648.2:n.-6G>A
XM_011526135.1:c.-6G>A	XP_011524437.1:n.-6G>A
XR_935246.1:n.1107G>A
XR_935247.1:n.1107G>A
XR_935248.1:n.886G>A
XM_011526135.3:c.-6G>A	XP_011524437.1:n.-6G>A
XM_017025917.2:c.-6G>A	XP_016881406.1:n.-6G>A
XR_935248.3:n.1388G>A
NM_000633.3:c.-6G>A MANE Select	NP_000624.2:n.-6G>A
NM_000657.3:c.-6G>A	NP_000648.2:n.-6G>A