Canonical Allele Identifier: CA991105602

Gene: BCL2

Linked Data

• dbSNP Id: rs1913601920
• gnomAD v3: 18-63318884-G-C
• gnomAD v4: 18-63318884-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318884G>C , CM000680.2:g.63318884G>C	GRCh38
NC_000018.9:g.60986117G>C , CM000680.1:g.60986117G>C	GRCh37
NC_000018.8:g.59137097G>C	NCBI36
NG_009361.1:g.5497C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-218C>G MANE Select	ENSP00000329623.3:n.-218C>G
ENST00000333681.4:c.-218C>G	ENSP00000329623.3:n.-218C>G
ENST00000398117.1:c.-218C>G	ENSP00000381185.1:n.-218C>G
NM_000633.2:c.-218C>G	NP_000624.2:n.-218C>G
NM_000657.2:c.-218C>G	NP_000648.2:n.-218C>G
XM_011526135.1:c.-218C>G	XP_011524437.1:n.-218C>G
XR_935246.1:n.895C>G
XR_935247.1:n.895C>G
XR_935248.1:n.674C>G
XM_011526135.3:c.-218C>G	XP_011524437.1:n.-218C>G
XM_017025917.2:c.-218C>G	XP_016881406.1:n.-218C>G
XR_935248.3:n.1176C>G
NM_000633.3:c.-218C>G MANE Select	NP_000624.2:n.-218C>G
NM_000657.3:c.-218C>G	NP_000648.2:n.-218C>G