Canonical Allele Identifier: CA302017037

Gene: BCL2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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