Canonical Allele Identifier: CA2308716817

Gene: BCL2

Linked Data

• dbSNP Id: rs1462129

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63313638T>A , CM000680.2:g.63313638T>A	GRCh38
NC_000018.9:g.60980871T>A , CM000680.1:g.60980871T>A	GRCh37
NC_000018.8:g.59131851T>A	NCBI36
NG_009361.1:g.10743A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000333681.5:c.585+4444A>T MANE Select	ENSP00000329623.3:n.585+4444A>T
ENST00000677227.1:c.585+4444A>T	ENSP00000504566.1:n.585+4444A>T
ENST00000678134.1:c.585+4444A>T	ENSP00000503628.1:n.585+4444A>T
ENST00000678349.1:c.1137+3892A>T	ENSP00000504190.1:n.1137+3892A>T
ENST00000333681.4:c.585+4444A>T	ENSP00000329623.3:n.585+4444A>T
ENST00000398117.1:c.585+4444A>T	ENSP00000381185.1:n.585+4444A>T
NM_000633.2:c.585+4444A>T	NP_000624.2:n.585+4444A>T
XM_011526135.1:c.585+4444A>T	XP_011524437.1:n.585+4444A>T
XR_935246.1:n.1697+4444A>T
XR_935247.1:n.1697+4444A>T
XR_935248.1:n.1476+4444A>T
XM_011526135.3:c.585+4444A>T	XP_011524437.1:n.585+4444A>T
XM_017025917.2:c.585+4444A>T	XP_016881406.1:n.585+4444A>T
XR_935248.3:n.1978+4444A>T
NM_000633.3:c.585+4444A>T MANE Select	NP_000624.2:n.585+4444A>T