Canonical Allele Identifier: CA2308672634
Community Standard Title: NM_000633.3(BCL2):c.586-84570C=
Gene: BCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63213329G= , CM000680.2:g.63213329G= GRCh38
NC_000018.9:g.60880562G= , CM000680.1:g.60880562G= GRCh37
NC_000018.8:g.59031542G= NCBI36
NG_009361.1:g.111052C=

Transcript Alleles

HGVS Amino-acid Change
NM_000633.3:c.586-84570C= MANE Select NP_000624.2:n.586-84570C=
ENST00000333681.5:c.586-84570C= MANE Select ENSP00000329623.3:n.586-84570C=
NM_000633.2:c.586-84570C= NP_000624.2:n.586-84570C=
ENST00000333681.4:c.586-84570C= ENSP00000329623.3:n.586-84570C=
ENST00000398117.1:c.586-84570C= ENSP00000381185.1:n.586-84570C=
ENST00000677227.1:c.913+67558C= ENSP00000504566.1:n.913+67558C=
ENST00000678134.1:c.790-84570C= ENSP00000503628.1:n.790-84570C=
ENST00000678349.1:c.1138-84570C= ENSP00000504190.1:n.1138-84570C=
XR_935246.1:n.2025+67558C=
XR_935248.1:n.1804+67558C=
XR_935248.3:n.2306+67558C=