Canonical Allele Identifier: CA657488314

Gene: BCL2

Linked Data

• gnomAD v4: 18-63318896-A-G
• COSMIC: COSN25419651

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318896A>G , CM000680.2:g.63318896A>G	GRCh38
NC_000018.9:g.60986129A>G , CM000680.1:g.60986129A>G	GRCh37
NC_000018.8:g.59137109A>G	NCBI36
NG_009361.1:g.5485T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-230T>C MANE Select	ENSP00000329623.3:n.-230T>C
ENST00000333681.4:c.-230T>C	ENSP00000329623.3:n.-230T>C
ENST00000398117.1:c.-230T>C	ENSP00000381185.1:n.-230T>C
NM_000633.2:c.-230T>C	NP_000624.2:n.-230T>C
NM_000657.2:c.-230T>C	NP_000648.2:n.-230T>C
XM_011526135.1:c.-230T>C	XP_011524437.1:n.-230T>C
XR_935246.1:n.883T>C
XR_935247.1:n.883T>C
XR_935248.1:n.662T>C
XM_011526135.3:c.-230T>C	XP_011524437.1:n.-230T>C
XM_017025917.2:c.-230T>C	XP_016881406.1:n.-230T>C
XR_935248.3:n.1164T>C
NM_000633.3:c.-230T>C MANE Select	NP_000624.2:n.-230T>C
NM_000657.3:c.-230T>C	NP_000648.2:n.-230T>C