Canonical Allele Identifier: CA2812775405
Gene: BCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63318927A>T , CM000680.2:g.63318927A>T GRCh38
NC_000018.9:g.60986160A>T , CM000680.1:g.60986160A>T GRCh37
NC_000018.8:g.59137140A>T NCBI36
NG_009361.1:g.5454T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000333681.5:c.-261T>A MANE Select ENSP00000329623.3:n.-261T>A
ENST00000333681.4:c.-261T>A ENSP00000329623.3:n.-261T>A
ENST00000398117.1:c.-261T>A ENSP00000381185.1:n.-261T>A
NM_000633.2:c.-261T>A NP_000624.2:n.-261T>A
NM_000657.2:c.-261T>A NP_000648.2:n.-261T>A
XM_011526135.1:c.-261T>A XP_011524437.1:n.-261T>A
XR_935246.1:n.852T>A
XR_935247.1:n.852T>A
XR_935248.1:n.631T>A
XM_011526135.3:c.-261T>A XP_011524437.1:n.-261T>A
XM_017025917.2:c.-261T>A XP_016881406.1:n.-261T>A
XR_935248.3:n.1133T>A
NM_000633.3:c.-261T>A MANE Select NP_000624.2:n.-261T>A
NM_000657.3:c.-261T>A NP_000648.2:n.-261T>A