Canonical Allele Identifier: CA2308702134

Gene: BCL2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63279851A= , CM000680.2:g.63279851A=	GRCh38
NC_000018.9:g.60947084A= , CM000680.1:g.60947084A=	GRCh37
NC_000018.8:g.59098064A=	NCBI36
NG_009361.1:g.44530T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.585+38231T= MANE Select	ENSP00000329623.3:n.585+38231T=
ENST00000677227.1:c.913+1036T=	ENSP00000504566.1:n.913+1036T=
ENST00000678134.1:c.789+21811T=	ENSP00000503628.1:n.789+21811T=
ENST00000678349.1:c.1137+37679T=	ENSP00000504190.1:n.1137+37679T=
ENST00000333681.4:c.585+38231T=	ENSP00000329623.3:n.585+38231T=
ENST00000398117.1:c.585+38231T=	ENSP00000381185.1:n.585+38231T=
NM_000633.2:c.585+38231T=	NP_000624.2:n.585+38231T=
XR_935246.1:n.2025+1036T=
XR_935247.1:n.2025+1036T=
XR_935248.1:n.1804+1036T=
XR_935248.3:n.2306+1036T=
NM_000633.3:c.585+38231T= MANE Select	NP_000624.2:n.585+38231T=