Canonical Allele Identifier: CA8985934

Gene: BCL2

Linked Data

• dbSNP Id: rs193014588
• ExAC: 18:60985900 C / T
• gnomAD v2: 18-60985900-C-T
• gnomAD v3: 18-63318667-C-T
• gnomAD v4: 18-63318667-C-T
• COSMIC: COSN25215786 ; COSN25312076 ; COSN25623849 ; COSN25663074
• MyVariant Identifiers: chr18:g.60985900C>T (hg19) ; chr18:g.63318667C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318667C>T , CM000680.2:g.63318667C>T	GRCh38
NC_000018.9:g.60985900C>T , CM000680.1:g.60985900C>T	GRCh37
NC_000018.8:g.59136880C>T	NCBI36
NG_009361.1:g.5714G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-1G>A MANE Select	ENSP00000329623.3:n.-1G>A
ENST00000333681.4:c.-1G>A	ENSP00000329623.3:n.-1G>A
ENST00000398117.1:c.-1G>A	ENSP00000381185.1:n.-1G>A
ENST00000589955.2:c.-1G>A	ENSP00000466417.1:n.-1G>A
NM_000633.2:c.-1G>A	NP_000624.2:n.-1G>A
NM_000657.2:c.-1G>A	NP_000648.2:n.-1G>A
XM_011526135.1:c.-1G>A	XP_011524437.1:n.-1G>A
XR_935246.1:n.1112G>A
XR_935247.1:n.1112G>A
XR_935248.1:n.891G>A
XM_011526135.3:c.-1G>A	XP_011524437.1:n.-1G>A
XM_017025917.2:c.-1G>A	XP_016881406.1:n.-1G>A
XR_935248.3:n.1393G>A
NM_000633.3:c.-1G>A MANE Select	NP_000624.2:n.-1G>A
NM_000657.3:c.-1G>A	NP_000648.2:n.-1G>A