Canonical Allele Identifier: CA2308718963
Gene: BCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63318904C= , CM000680.2:g.63318904C= GRCh38
NC_000018.9:g.60986137C= , CM000680.1:g.60986137C= GRCh37
NC_000018.8:g.59137117C= NCBI36
NG_009361.1:g.5477G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333681.5:c.-238G= MANE Select ENSP00000329623.3:n.-238G=
ENST00000333681.4:c.-238G= ENSP00000329623.3:n.-238G=
ENST00000398117.1:c.-238G= ENSP00000381185.1:n.-238G=
NM_000633.2:c.-238G= NP_000624.2:n.-238G=
NM_000657.2:c.-238G= NP_000648.2:n.-238G=
XM_011526135.1:c.-238G= XP_011524437.1:n.-238G=
XR_935246.1:n.875G=
XR_935247.1:n.875G=
XR_935248.1:n.654G=
XM_011526135.3:c.-238G= XP_011524437.1:n.-238G=
XM_017025917.2:c.-238G= XP_016881406.1:n.-238G=
XR_935248.3:n.1156G=
NM_000633.3:c.-238G= MANE Select NP_000624.2:n.-238G=
NM_000657.3:c.-238G= NP_000648.2:n.-238G=