Canonical Allele Identifier: CA2308706802

Gene: BCL2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63291394C= , CM000680.2:g.63291394C=	GRCh38
NC_000018.9:g.60958627C= , CM000680.1:g.60958627C=	GRCh37
NC_000018.8:g.59109607C=	NCBI36
NG_009361.1:g.32987G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000333681.5:c.585+26688G= MANE Select	ENSP00000329623.3:n.585+26688G=
ENST00000677227.1:c.586-10180G=	ENSP00000504566.1:n.586-10180G=
ENST00000678134.1:c.789+10268G=	ENSP00000503628.1:n.789+10268G=
ENST00000678349.1:c.1137+26136G=	ENSP00000504190.1:n.1137+26136G=
ENST00000333681.4:c.585+26688G=	ENSP00000329623.3:n.585+26688G=
ENST00000398117.1:c.585+26688G=	ENSP00000381185.1:n.585+26688G=
NM_000633.2:c.585+26688G=	NP_000624.2:n.585+26688G=
XR_935246.1:n.1698-10180G=
XR_935247.1:n.1698-10180G=
XR_935248.1:n.1477-10180G=
XR_935248.3:n.1979-10180G=
NM_000633.3:c.585+26688G= MANE Select	NP_000624.2:n.585+26688G=