Canonical Allele Identifier: CA8985932
Gene: BCL2 HGNC NCBI

Linked Data

dbSNP Id: rs557714365

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63318659T>C , CM000680.2:g.63318659T>C GRCh38
NC_000018.9:g.60985892T>C , CM000680.1:g.60985892T>C GRCh37
NC_000018.8:g.59136872T>C NCBI36
NG_009361.1:g.5722A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000333681.5:c.8A>G MANE Select ENSP00000329623.3:p.His3Arg
ENST00000677227.1:c.8A>G ENSP00000504566.1:p.His3Arg
ENST00000678134.1:c.8A>G ENSP00000503628.1:p.His3Arg
ENST00000678349.1:c.8A>G ENSP00000504190.1:p.His3Arg
ENST00000333681.4:c.8A>G ENSP00000329623.3:p.His3Arg
ENST00000398117.1:c.8A>G ENSP00000381185.1:p.His3Arg
ENST00000589955.2:c.8A>G ENSP00000466417.1:p.His3Arg
NM_000633.2:c.8A>G NP_000624.2:p.His3Arg
NM_000657.2:c.8A>G NP_000648.2:p.His3Arg
XM_011526135.1:c.8A>G XP_011524437.1:p.His3Arg
XR_935246.1:n.1120A>G
XR_935247.1:n.1120A>G
XR_935248.1:n.899A>G
XM_011526135.3:c.8A>G XP_011524437.1:p.His3Arg
XM_017025917.2:c.8A>G XP_016881406.1:p.His3Arg
XR_935248.3:n.1401A>G
NM_000633.3:c.8A>G MANE Select NP_000624.2:p.His3Arg
NM_000657.3:c.8A>G NP_000648.2:p.His3Arg