Canonical Allele Identifier: CA991090631
Gene: BCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63127841C>G , CM000680.2:g.63127841C>G GRCh38
NC_000018.9:g.60795074C>G , CM000680.1:g.60795074C>G GRCh37
NC_000018.8:g.58946054C>G NCBI36
NG_009361.1:g.196540G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000333681.5:c.*784G>C MANE Select ENSP00000329623.3:n.*784G>C
ENST00000677227.1:c.1832G>C ENSP00000504566.1:n.1832G>C
ENST00000677635.1:n.1068G>C
ENST00000678134.1:c.1708G>C ENSP00000503628.1:n.1708G>C
ENST00000678301.1:c.*784G>C ENSP00000504546.1:n.*784G>C
ENST00000678349.1:c.2056G>C ENSP00000504190.1:n.2056G>C
ENST00000333681.4:c.*784G>C ENSP00000329623.3:n.*784G>C
ENST00000398117.1:c.*784G>C ENSP00000381185.1:n.*784G>C
NM_000633.2:c.*784G>C NP_000624.2:n.*784G>C
NM_000633.3:c.*784G>C MANE Select NP_000624.2:n.*784G>C