Canonical Allele Identifier: CA2308702129

Gene: BCL2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63279831T= , CM000680.2:g.63279831T=	GRCh38
NC_000018.9:g.60947064T= , CM000680.1:g.60947064T=	GRCh37
NC_000018.8:g.59098044T=	NCBI36
NG_009361.1:g.44550A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.585+38251A= MANE Select	ENSP00000329623.3:n.585+38251A=
ENST00000677227.1:c.913+1056A=	ENSP00000504566.1:n.913+1056A=
ENST00000678134.1:c.789+21831A=	ENSP00000503628.1:n.789+21831A=
ENST00000678349.1:c.1137+37699A=	ENSP00000504190.1:n.1137+37699A=
ENST00000333681.4:c.585+38251A=	ENSP00000329623.3:n.585+38251A=
ENST00000398117.1:c.585+38251A=	ENSP00000381185.1:n.585+38251A=
NM_000633.2:c.585+38251A=	NP_000624.2:n.585+38251A=
XR_935246.1:n.2025+1056A=
XR_935247.1:n.2025+1056A=
XR_935248.1:n.1804+1056A=
XR_935248.3:n.2306+1056A=
NM_000633.3:c.585+38251A= MANE Select	NP_000624.2:n.585+38251A=