Canonical Allele Identifier: CA2308644529

Gene: BCL2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63153272T= , CM000680.2:g.63153272T=	GRCh38
NC_000018.9:g.60820505T= , CM000680.1:g.60820505T=	GRCh37
NC_000018.8:g.58971485T=	NCBI36
NG_009361.1:g.171109A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000333681.5:c.586-24513A= MANE Select	ENSP00000329623.3:n.586-24513A=
ENST00000677227.1:c.914-24513A=	ENSP00000504566.1:n.914-24513A=
ENST00000678134.1:c.790-24513A=	ENSP00000503628.1:n.790-24513A=
ENST00000678301.1:c.24+4801A=	ENSP00000504546.1:n.24+4801A=
ENST00000678349.1:c.1138-24513A=	ENSP00000504190.1:n.1138-24513A=
ENST00000333681.4:c.586-24513A=	ENSP00000329623.3:n.586-24513A=
ENST00000398117.1:c.586-24513A=	ENSP00000381185.1:n.586-24513A=
ENST00000590515.1:n.24+8574A=
NM_000633.2:c.586-24513A=	NP_000624.2:n.586-24513A=
XR_935246.1:n.2026-24513A=
XR_935248.1:n.1805-24513A=
XR_935248.3:n.2307-24513A=
NM_000633.3:c.586-24513A= MANE Select	NP_000624.2:n.586-24513A=