Canonical Allele Identifier: CA2308644522

Gene: BCL2

Linked Data

• dbSNP Id: rs1568217376

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63153250A>G , CM000680.2:g.63153250A>G	GRCh38
NC_000018.9:g.60820483A>G , CM000680.1:g.60820483A>G	GRCh37
NC_000018.8:g.58971463A>G	NCBI36
NG_009361.1:g.171131T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000333681.5:c.586-24491T>C MANE Select	ENSP00000329623.3:n.586-24491T>C
ENST00000677227.1:c.914-24491T>C	ENSP00000504566.1:n.914-24491T>C
ENST00000678134.1:c.790-24491T>C	ENSP00000503628.1:n.790-24491T>C
ENST00000678301.1:c.24+4823T>C	ENSP00000504546.1:n.24+4823T>C
ENST00000678349.1:c.1138-24491T>C	ENSP00000504190.1:n.1138-24491T>C
ENST00000333681.4:c.586-24491T>C	ENSP00000329623.3:n.586-24491T>C
ENST00000398117.1:c.586-24491T>C	ENSP00000381185.1:n.586-24491T>C
ENST00000590515.1:n.24+8596T>C
NM_000633.2:c.586-24491T>C	NP_000624.2:n.586-24491T>C
XR_935246.1:n.2026-24491T>C
XR_935248.1:n.1805-24491T>C
XR_935248.3:n.2307-24491T>C
NM_000633.3:c.586-24491T>C MANE Select	NP_000624.2:n.586-24491T>C