Canonical Allele Identifier: CA2581353380

Gene: BCL2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63311780G>T , CM000680.2:g.63311780G>T	GRCh38
NC_000018.9:g.60979013G>T , CM000680.1:g.60979013G>T	GRCh37
NC_000018.8:g.59129993G>T	NCBI36
NG_009361.1:g.12601C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000633.3:c.585+6302C>A MANE Select	NP_000624.2:n.585+6302C>A
ENST00000333681.5:c.585+6302C>A MANE Select	ENSP00000329623.3:n.585+6302C>A
NM_000633.2:c.585+6302C>A	NP_000624.2:n.585+6302C>A
ENST00000333681.4:c.585+6302C>A	ENSP00000329623.3:n.585+6302C>A
ENST00000398117.1:c.585+6302C>A	ENSP00000381185.1:n.585+6302C>A
ENST00000677227.1:c.585+6302C>A	ENSP00000504566.1:n.585+6302C>A
ENST00000678134.1:c.585+6302C>A	ENSP00000503628.1:n.585+6302C>A
ENST00000678349.1:c.1137+5750C>A	ENSP00000504190.1:n.1137+5750C>A
XM_011526135.1:c.585+6302C>A	XP_011524437.1:n.585+6302C>A
XM_011526135.3:c.585+6302C>A	XP_011524437.1:n.585+6302C>A
XM_017025917.2:c.585+6302C>A	XP_016881406.1:n.585+6302C>A
XR_935246.1:n.1697+6302C>A
XR_935247.1:n.1697+6302C>A
XR_935248.1:n.1476+6302C>A
XR_935248.3:n.1978+6302C>A