Canonical Allele Identifier: CA781350085

Gene: BCL2

Linked Data

• dbSNP Id: rs1273914340
• gnomAD v3: 18-63153298-G-T
• gnomAD v4: 18-63153298-G-T
• MyVariant Identifiers: chr18:g.60820531G>T (hg19) ; chr18:g.63153298G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63153298G>T , CM000680.2:g.63153298G>T	GRCh38
NC_000018.9:g.60820531G>T , CM000680.1:g.60820531G>T	GRCh37
NC_000018.8:g.58971511G>T	NCBI36
NG_009361.1:g.171083C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.586-24539C>A MANE Select	ENSP00000329623.3:n.586-24539C>A
ENST00000677227.1:c.914-24539C>A	ENSP00000504566.1:n.914-24539C>A
ENST00000678134.1:c.790-24539C>A	ENSP00000503628.1:n.790-24539C>A
ENST00000678301.1:c.24+4775C>A	ENSP00000504546.1:n.24+4775C>A
ENST00000678349.1:c.1138-24539C>A	ENSP00000504190.1:n.1138-24539C>A
ENST00000333681.4:c.586-24539C>A	ENSP00000329623.3:n.586-24539C>A
ENST00000398117.1:c.586-24539C>A	ENSP00000381185.1:n.586-24539C>A
ENST00000590515.1:n.24+8548C>A
NM_000633.2:c.586-24539C>A	NP_000624.2:n.586-24539C>A
XR_935246.1:n.2026-24539C>A
XR_935248.1:n.1805-24539C>A
XR_935248.3:n.2307-24539C>A
NM_000633.3:c.586-24539C>A MANE Select	NP_000624.2:n.586-24539C>A