Canonical Allele Identifier: CA2308672105
Gene: BCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63212453C= , CM000680.2:g.63212453C= GRCh38
NC_000018.9:g.60879686C= , CM000680.1:g.60879686C= GRCh37
NC_000018.8:g.59030666C= NCBI36
NG_009361.1:g.111928G=

Transcript Alleles

HGVS Amino-acid Change
NM_000633.3:c.586-83694G= MANE Select NP_000624.2:n.586-83694G=
ENST00000333681.5:c.586-83694G= MANE Select ENSP00000329623.3:n.586-83694G=
NM_000633.2:c.586-83694G= NP_000624.2:n.586-83694G=
ENST00000333681.4:c.586-83694G= ENSP00000329623.3:n.586-83694G=
ENST00000398117.1:c.586-83694G= ENSP00000381185.1:n.586-83694G=
ENST00000677227.1:c.913+68434G= ENSP00000504566.1:n.913+68434G=
ENST00000678134.1:c.790-83694G= ENSP00000503628.1:n.790-83694G=
ENST00000678349.1:c.1138-83694G= ENSP00000504190.1:n.1138-83694G=
XR_935246.1:n.2025+68434G=
XR_935248.1:n.1804+68434G=
XR_935248.3:n.2306+68434G=