Canonical Allele Identifier: CA657488094

Gene: BCL2

Linked Data

• gnomAD v4: 18-63318778-C-G
• COSMIC: COSN25054344

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318778C>G , CM000680.2:g.63318778C>G	GRCh38
NC_000018.9:g.60986011C>G , CM000680.1:g.60986011C>G	GRCh37
NC_000018.8:g.59136991C>G	NCBI36
NG_009361.1:g.5603G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-112G>C MANE Select	ENSP00000329623.3:n.-112G>C
ENST00000333681.4:c.-112G>C	ENSP00000329623.3:n.-112G>C
ENST00000398117.1:c.-112G>C	ENSP00000381185.1:n.-112G>C
ENST00000589955.2:c.-112G>C	ENSP00000466417.1:n.-112G>C
NM_000633.2:c.-112G>C	NP_000624.2:n.-112G>C
NM_000657.2:c.-112G>C	NP_000648.2:n.-112G>C
XM_011526135.1:c.-112G>C	XP_011524437.1:n.-112G>C
XR_935246.1:n.1001G>C
XR_935247.1:n.1001G>C
XR_935248.1:n.780G>C
XM_011526135.3:c.-112G>C	XP_011524437.1:n.-112G>C
XM_017025917.2:c.-112G>C	XP_016881406.1:n.-112G>C
XR_935248.3:n.1282G>C
NM_000633.3:c.-112G>C MANE Select	NP_000624.2:n.-112G>C
NM_000657.3:c.-112G>C	NP_000648.2:n.-112G>C