Canonical Allele Identifier: CA657488059

Gene: BCL2

Linked Data

• gnomAD v4: 18-63318767-T-C
• COSMIC: COSN25397259

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318767T>C , CM000680.2:g.63318767T>C	GRCh38
NC_000018.9:g.60986000T>C , CM000680.1:g.60986000T>C	GRCh37
NC_000018.8:g.59136980T>C	NCBI36
NG_009361.1:g.5614A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-101A>G MANE Select	ENSP00000329623.3:n.-101A>G
ENST00000333681.4:c.-101A>G	ENSP00000329623.3:n.-101A>G
ENST00000398117.1:c.-101A>G	ENSP00000381185.1:n.-101A>G
ENST00000589955.2:c.-101A>G	ENSP00000466417.1:n.-101A>G
NM_000633.2:c.-101A>G	NP_000624.2:n.-101A>G
NM_000657.2:c.-101A>G	NP_000648.2:n.-101A>G
XM_011526135.1:c.-101A>G	XP_011524437.1:n.-101A>G
XR_935246.1:n.1012A>G
XR_935247.1:n.1012A>G
XR_935248.1:n.791A>G
XM_011526135.3:c.-101A>G	XP_011524437.1:n.-101A>G
XM_017025917.2:c.-101A>G	XP_016881406.1:n.-101A>G
XR_935248.3:n.1293A>G
NM_000633.3:c.-101A>G MANE Select	NP_000624.2:n.-101A>G
NM_000657.3:c.-101A>G	NP_000648.2:n.-101A>G