Canonical Allele Identifier: CA630132762

Gene: BCL2

Linked Data

• dbSNP Id: rs1357914547
• gnomAD v2: 18-60986170-T-G
• gnomAD v3: 18-63318937-T-G
• gnomAD v4: 18-63318937-T-G
• MyVariant Identifiers: chr18:g.60986170T>G (hg19) ; chr18:g.63318937T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318937T>G , CM000680.2:g.63318937T>G	GRCh38
NC_000018.9:g.60986170T>G , CM000680.1:g.60986170T>G	GRCh37
NC_000018.8:g.59137150T>G	NCBI36
NG_009361.1:g.5444A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-271A>C MANE Select	ENSP00000329623.3:n.-271A>C
ENST00000333681.4:c.-271A>C	ENSP00000329623.3:n.-271A>C
ENST00000398117.1:c.-271A>C	ENSP00000381185.1:n.-271A>C
NM_000633.2:c.-271A>C	NP_000624.2:n.-271A>C
NM_000657.2:c.-271A>C	NP_000648.2:n.-271A>C
XM_011526135.1:c.-271A>C	XP_011524437.1:n.-271A>C
XR_935246.1:n.842A>C
XR_935247.1:n.842A>C
XR_935248.1:n.621A>C
XM_011526135.3:c.-271A>C	XP_011524437.1:n.-271A>C
XM_017025917.2:c.-271A>C	XP_016881406.1:n.-271A>C
XR_935248.3:n.1123A>C
NM_000633.3:c.-271A>C MANE Select	NP_000624.2:n.-271A>C
NM_000657.3:c.-271A>C	NP_000648.2:n.-271A>C