Canonical Allele Identifier: CA2308706807
Gene: BCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63291411A= , CM000680.2:g.63291411A= GRCh38
NC_000018.9:g.60958644A= , CM000680.1:g.60958644A= GRCh37
NC_000018.8:g.59109624A= NCBI36
NG_009361.1:g.32970T=

Transcript Alleles

HGVS Amino-acid Change
NM_000633.3:c.585+26671T= MANE Select NP_000624.2:n.585+26671T=
ENST00000333681.5:c.585+26671T= MANE Select ENSP00000329623.3:n.585+26671T=
NM_000633.2:c.585+26671T= NP_000624.2:n.585+26671T=
ENST00000333681.4:c.585+26671T= ENSP00000329623.3:n.585+26671T=
ENST00000398117.1:c.585+26671T= ENSP00000381185.1:n.585+26671T=
ENST00000677227.1:c.586-10197T= ENSP00000504566.1:n.586-10197T=
ENST00000678134.1:c.789+10251T= ENSP00000503628.1:n.789+10251T=
ENST00000678349.1:c.1137+26119T= ENSP00000504190.1:n.1137+26119T=
XR_935246.1:n.1698-10197T=
XR_935247.1:n.1698-10197T=
XR_935248.1:n.1477-10197T=
XR_935248.3:n.1979-10197T=