Canonical Allele Identifier: CA2308718960
Gene: BCL2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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