Canonical Allele Identifier: CA781360481
Gene: BCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63178651T>A , CM000680.2:g.63178651T>A GRCh38
NC_000018.9:g.60845884T>A , CM000680.1:g.60845884T>A GRCh37
NC_000018.8:g.58996864T>A NCBI36
NG_009361.1:g.145730A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000333681.5:c.586-49892A>T MANE Select ENSP00000329623.3:n.586-49892A>T
ENST00000677227.1:c.914-49892A>T ENSP00000504566.1:n.914-49892A>T
ENST00000678134.1:c.790-49892A>T ENSP00000503628.1:n.790-49892A>T
ENST00000678349.1:c.1138-49892A>T ENSP00000504190.1:n.1138-49892A>T
ENST00000333681.4:c.586-49892A>T ENSP00000329623.3:n.586-49892A>T
ENST00000398117.1:c.586-49892A>T ENSP00000381185.1:n.586-49892A>T
NM_000633.2:c.586-49892A>T NP_000624.2:n.586-49892A>T
XR_935246.1:n.2026-49892A>T
XR_935248.1:n.1805-49892A>T
XR_935248.3:n.2307-49892A>T
NM_000633.3:c.586-49892A>T MANE Select NP_000624.2:n.586-49892A>T