Canonical Allele Identifier: CA402633296

Gene: BCL2

Linked Data

• gnomAD v4: 18-63318657-C-G
• COSMIC: COSM564100 ; COSM564101 ; COSM1649430
• MyVariant Identifiers: chr18:g.60985890C>G (hg19) ; chr18:g.63318657C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318657C>G , CM000680.2:g.63318657C>G	GRCh38
NC_000018.9:g.60985890C>G , CM000680.1:g.60985890C>G	GRCh37
NC_000018.8:g.59136870C>G	NCBI36
NG_009361.1:g.5724G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.10G>C MANE Select	ENSP00000329623.3:p.Ala4Pro
ENST00000677227.1:c.10G>C	ENSP00000504566.1:p.Ala4Pro
ENST00000678134.1:c.10G>C	ENSP00000503628.1:p.Ala4Pro
ENST00000678349.1:c.10G>C	ENSP00000504190.1:p.Ala4Pro
ENST00000333681.4:c.10G>C	ENSP00000329623.3:p.Ala4Pro
ENST00000398117.1:c.10G>C	ENSP00000381185.1:p.Ala4Pro
ENST00000589955.2:c.10G>C	ENSP00000466417.1:p.Ala4Pro
NM_000633.2:c.10G>C	NP_000624.2:p.Ala4Pro
NM_000657.2:c.10G>C	NP_000648.2:p.Ala4Pro
XM_011526135.1:c.10G>C	XP_011524437.1:p.Ala4Pro
XR_935246.1:n.1122G>C
XR_935247.1:n.1122G>C
XR_935248.1:n.901G>C
XM_011526135.3:c.10G>C	XP_011524437.1:p.Ala4Pro
XM_017025917.2:c.10G>C	XP_016881406.1:p.Ala4Pro
XR_935248.3:n.1403G>C
NM_000633.3:c.10G>C MANE Select	NP_000624.2:p.Ala4Pro
NM_000657.3:c.10G>C	NP_000648.2:p.Ala4Pro