Canonical Allele Identifier: CA2308662162

Gene: BCL2

Linked Data

• dbSNP Id: rs899967

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63192088C>A , CM000680.2:g.63192088C>A	GRCh38
NC_000018.9:g.60859321C>A , CM000680.1:g.60859321C>A	GRCh37
NC_000018.8:g.59010301C>A	NCBI36
NG_009361.1:g.132293G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000333681.5:c.586-63329G>T MANE Select	ENSP00000329623.3:n.586-63329G>T
ENST00000677227.1:c.914-63329G>T	ENSP00000504566.1:n.914-63329G>T
ENST00000678134.1:c.790-63329G>T	ENSP00000503628.1:n.790-63329G>T
ENST00000678349.1:c.1138-63329G>T	ENSP00000504190.1:n.1138-63329G>T
ENST00000333681.4:c.586-63329G>T	ENSP00000329623.3:n.586-63329G>T
ENST00000398117.1:c.586-63329G>T	ENSP00000381185.1:n.586-63329G>T
NM_000633.2:c.586-63329G>T	NP_000624.2:n.586-63329G>T
XR_935246.1:n.2026-63329G>T
XR_935248.1:n.1805-63329G>T
XR_935248.3:n.2307-63329G>T
NM_000633.3:c.586-63329G>T MANE Select	NP_000624.2:n.586-63329G>T