Canonical Allele Identifier: CA781350117

Gene: BCL2

Linked Data

• dbSNP Id: rs1319626913
• MyVariant Identifiers: chr18:g.60820611C>T (hg19) ; chr18:g.63153378C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63153378C>T , CM000680.2:g.63153378C>T	GRCh38
NC_000018.9:g.60820611C>T , CM000680.1:g.60820611C>T	GRCh37
NC_000018.8:g.58971591C>T	NCBI36
NG_009361.1:g.171003G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.586-24619G>A MANE Select	ENSP00000329623.3:n.586-24619G>A
ENST00000677227.1:c.914-24619G>A	ENSP00000504566.1:n.914-24619G>A
ENST00000678134.1:c.790-24619G>A	ENSP00000503628.1:n.790-24619G>A
ENST00000678301.1:c.24+4695G>A	ENSP00000504546.1:n.24+4695G>A
ENST00000678349.1:c.1138-24619G>A	ENSP00000504190.1:n.1138-24619G>A
ENST00000333681.4:c.586-24619G>A	ENSP00000329623.3:n.586-24619G>A
ENST00000398117.1:c.586-24619G>A	ENSP00000381185.1:n.586-24619G>A
ENST00000590515.1:n.24+8468G>A
NM_000633.2:c.586-24619G>A	NP_000624.2:n.586-24619G>A
XR_935246.1:n.2026-24619G>A
XR_935248.1:n.1805-24619G>A
XR_935248.3:n.2307-24619G>A
NM_000633.3:c.586-24619G>A MANE Select	NP_000624.2:n.586-24619G>A