Canonical Allele Identifier: CA2576520009
Gene: BCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63318913T>A , CM000680.2:g.63318913T>A GRCh38
NC_000018.9:g.60986146T>A , CM000680.1:g.60986146T>A GRCh37
NC_000018.8:g.59137126T>A NCBI36
NG_009361.1:g.5468A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000333681.5:c.-247A>T MANE Select ENSP00000329623.3:n.-247A>T
ENST00000333681.4:c.-247A>T ENSP00000329623.3:n.-247A>T
ENST00000398117.1:c.-247A>T ENSP00000381185.1:n.-247A>T
NM_000633.2:c.-247A>T NP_000624.2:n.-247A>T
NM_000657.2:c.-247A>T NP_000648.2:n.-247A>T
XM_011526135.1:c.-247A>T XP_011524437.1:n.-247A>T
XR_935246.1:n.866A>T
XR_935247.1:n.866A>T
XR_935248.1:n.645A>T
XM_011526135.3:c.-247A>T XP_011524437.1:n.-247A>T
XM_017025917.2:c.-247A>T XP_016881406.1:n.-247A>T
XR_935248.3:n.1147A>T
NM_000633.3:c.-247A>T MANE Select NP_000624.2:n.-247A>T
NM_000657.3:c.-247A>T NP_000648.2:n.-247A>T