Canonical Allele Identifier: CA2308644561
Gene: BCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63153343A= , CM000680.2:g.63153343A= GRCh38
NC_000018.9:g.60820576A= , CM000680.1:g.60820576A= GRCh37
NC_000018.8:g.58971556A= NCBI36
NG_009361.1:g.171038T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333681.5:c.586-24584T= MANE Select ENSP00000329623.3:n.586-24584T=
ENST00000677227.1:c.914-24584T= ENSP00000504566.1:n.914-24584T=
ENST00000678134.1:c.790-24584T= ENSP00000503628.1:n.790-24584T=
ENST00000678301.1:c.24+4730T= ENSP00000504546.1:n.24+4730T=
ENST00000678349.1:c.1138-24584T= ENSP00000504190.1:n.1138-24584T=
ENST00000333681.4:c.586-24584T= ENSP00000329623.3:n.586-24584T=
ENST00000398117.1:c.586-24584T= ENSP00000381185.1:n.586-24584T=
ENST00000590515.1:n.24+8503T=
NM_000633.2:c.586-24584T= NP_000624.2:n.586-24584T=
XR_935246.1:n.2026-24584T=
XR_935248.1:n.1805-24584T=
XR_935248.3:n.2307-24584T=
NM_000633.3:c.586-24584T= MANE Select NP_000624.2:n.586-24584T=