Canonical Allele Identifier: CA402633276

Gene: BCL2

Linked Data

• COSMIC: COSM220918 ; COSM220919
• MyVariant Identifiers: chr18:g.60985880G>T (hg19) ; chr18:g.63318647G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318647G>T , CM000680.2:g.63318647G>T	GRCh38
NC_000018.9:g.60985880G>T , CM000680.1:g.60985880G>T	GRCh37
NC_000018.8:g.59136860G>T	NCBI36
NG_009361.1:g.5734C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000333681.5:c.20C>A MANE Select	ENSP00000329623.3:p.Thr7Lys
ENST00000677227.1:c.20C>A	ENSP00000504566.1:p.Thr7Lys
ENST00000678134.1:c.20C>A	ENSP00000503628.1:p.Thr7Lys
ENST00000678349.1:c.20C>A	ENSP00000504190.1:p.Thr7Lys
ENST00000333681.4:c.20C>A	ENSP00000329623.3:p.Thr7Lys
ENST00000398117.1:c.20C>A	ENSP00000381185.1:p.Thr7Lys
ENST00000589955.2:c.20C>A	ENSP00000466417.1:p.Thr7Lys
NM_000633.2:c.20C>A	NP_000624.2:p.Thr7Lys
NM_000657.2:c.20C>A	NP_000648.2:p.Thr7Lys
XM_011526135.1:c.20C>A	XP_011524437.1:p.Thr7Lys
XR_935246.1:n.1132C>A
XR_935247.1:n.1132C>A
XR_935248.1:n.911C>A
XM_011526135.3:c.20C>A	XP_011524437.1:p.Thr7Lys
XM_017025917.2:c.20C>A	XP_016881406.1:p.Thr7Lys
XR_935248.3:n.1413C>A
NM_000633.3:c.20C>A MANE Select	NP_000624.2:p.Thr7Lys
NM_000657.3:c.20C>A	NP_000648.2:p.Thr7Lys