Canonical Allele Identifier: CA2812775397
Gene: BCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63318681A>C , CM000680.2:g.63318681A>C GRCh38
NC_000018.9:g.60985914A>C , CM000680.1:g.60985914A>C GRCh37
NC_000018.8:g.59136894A>C NCBI36
NG_009361.1:g.5700T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000333681.5:c.-15T>G MANE Select ENSP00000329623.3:n.-15T>G
ENST00000333681.4:c.-15T>G ENSP00000329623.3:n.-15T>G
ENST00000398117.1:c.-15T>G ENSP00000381185.1:n.-15T>G
ENST00000589955.2:c.-15T>G ENSP00000466417.1:n.-15T>G
NM_000633.2:c.-15T>G NP_000624.2:n.-15T>G
NM_000657.2:c.-15T>G NP_000648.2:n.-15T>G
XM_011526135.1:c.-15T>G XP_011524437.1:n.-15T>G
XR_935246.1:n.1098T>G
XR_935247.1:n.1098T>G
XR_935248.1:n.877T>G
XM_011526135.3:c.-15T>G XP_011524437.1:n.-15T>G
XM_017025917.2:c.-15T>G XP_016881406.1:n.-15T>G
XR_935248.3:n.1379T>G
NM_000633.3:c.-15T>G MANE Select NP_000624.2:n.-15T>G
NM_000657.3:c.-15T>G NP_000648.2:n.-15T>G