Canonical Allele Identifier: CA504301566

Gene: BCL2

Linked Data

• MyVariant Identifiers: chr18:g.60985888A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318655A>C , CM000680.2:g.63318655A>C	GRCh38
NC_000018.9:g.60985888A>C , CM000680.1:g.60985888A>C	GRCh37
NC_000018.8:g.59136868A>C	NCBI36
NG_009361.1:g.5726T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000333681.5:c.12T>G MANE Select	ENSP00000329623.3:p.Ala4=
ENST00000677227.1:c.12T>G	ENSP00000504566.1:p.Ala4=
ENST00000678134.1:c.12T>G	ENSP00000503628.1:p.Ala4=
ENST00000678349.1:c.12T>G	ENSP00000504190.1:p.Ala4=
ENST00000333681.4:c.12T>G	ENSP00000329623.3:p.Ala4=
ENST00000398117.1:c.12T>G	ENSP00000381185.1:p.Ala4=
ENST00000589955.2:c.12T>G	ENSP00000466417.1:p.Ala4=
NM_000633.2:c.12T>G	NP_000624.2:p.Ala4=
NM_000657.2:c.12T>G	NP_000648.2:p.Ala4=
XM_011526135.1:c.12T>G	XP_011524437.1:p.Ala4=
XR_935246.1:n.1124T>G
XR_935247.1:n.1124T>G
XR_935248.1:n.903T>G
XM_011526135.3:c.12T>G	XP_011524437.1:p.Ala4=
XM_017025917.2:c.12T>G	XP_016881406.1:p.Ala4=
XR_935248.3:n.1405T>G
NM_000633.3:c.12T>G MANE Select	NP_000624.2:p.Ala4=
NM_000657.3:c.12T>G	NP_000648.2:p.Ala4=