Canonical Allele Identifier: CA657213385

Gene: BCL2

Linked Data

• COSMIC: COSN6130385

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63153397G>A , CM000680.2:g.63153397G>A	GRCh38
NC_000018.9:g.60820630G>A , CM000680.1:g.60820630G>A	GRCh37
NC_000018.8:g.58971610G>A	NCBI36
NG_009361.1:g.170984C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.586-24638C>T MANE Select	ENSP00000329623.3:n.586-24638C>T
ENST00000677227.1:c.914-24638C>T	ENSP00000504566.1:n.914-24638C>T
ENST00000678134.1:c.790-24638C>T	ENSP00000503628.1:n.790-24638C>T
ENST00000678301.1:c.24+4676C>T	ENSP00000504546.1:n.24+4676C>T
ENST00000678349.1:c.1138-24638C>T	ENSP00000504190.1:n.1138-24638C>T
ENST00000333681.4:c.586-24638C>T	ENSP00000329623.3:n.586-24638C>T
ENST00000398117.1:c.586-24638C>T	ENSP00000381185.1:n.586-24638C>T
ENST00000590515.1:n.24+8449C>T
NM_000633.2:c.586-24638C>T	NP_000624.2:n.586-24638C>T
XR_935246.1:n.2026-24638C>T
XR_935248.1:n.1805-24638C>T
XR_935248.3:n.2307-24638C>T
NM_000633.3:c.586-24638C>T MANE Select	NP_000624.2:n.586-24638C>T