Canonical Allele Identifier: CA2308644560

Gene: BCL2

Linked Data

• dbSNP Id: rs956572

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63153338A>T , CM000680.2:g.63153338A>T	GRCh38
NC_000018.9:g.60820571A>T , CM000680.1:g.60820571A>T	GRCh37
NC_000018.8:g.58971551A>T	NCBI36
NG_009361.1:g.171043T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000333681.5:c.586-24579T>A MANE Select	ENSP00000329623.3:n.586-24579T>A
ENST00000677227.1:c.914-24579T>A	ENSP00000504566.1:n.914-24579T>A
ENST00000678134.1:c.790-24579T>A	ENSP00000503628.1:n.790-24579T>A
ENST00000678301.1:c.24+4735T>A	ENSP00000504546.1:n.24+4735T>A
ENST00000678349.1:c.1138-24579T>A	ENSP00000504190.1:n.1138-24579T>A
ENST00000333681.4:c.586-24579T>A	ENSP00000329623.3:n.586-24579T>A
ENST00000398117.1:c.586-24579T>A	ENSP00000381185.1:n.586-24579T>A
ENST00000590515.1:n.24+8508T>A
NM_000633.2:c.586-24579T>A	NP_000624.2:n.586-24579T>A
XR_935246.1:n.2026-24579T>A
XR_935248.1:n.1805-24579T>A
XR_935248.3:n.2307-24579T>A
NM_000633.3:c.586-24579T>A MANE Select	NP_000624.2:n.586-24579T>A