Canonical Allele Identifier: CA302010271

Gene: BCL2

Linked Data

• dbSNP Id: rs905039330
• gnomAD v3: 18-63153395-T-C
• gnomAD v4: 18-63153395-T-C
• MyVariant Identifiers: chr18:g.60820628T>C (hg19) ; chr18:g.63153395T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63153395T>C , CM000680.2:g.63153395T>C	GRCh38
NC_000018.9:g.60820628T>C , CM000680.1:g.60820628T>C	GRCh37
NC_000018.8:g.58971608T>C	NCBI36
NG_009361.1:g.170986A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.586-24636A>G MANE Select	ENSP00000329623.3:n.586-24636A>G
ENST00000677227.1:c.914-24636A>G	ENSP00000504566.1:n.914-24636A>G
ENST00000678134.1:c.790-24636A>G	ENSP00000503628.1:n.790-24636A>G
ENST00000678301.1:c.24+4678A>G	ENSP00000504546.1:n.24+4678A>G
ENST00000678349.1:c.1138-24636A>G	ENSP00000504190.1:n.1138-24636A>G
ENST00000333681.4:c.586-24636A>G	ENSP00000329623.3:n.586-24636A>G
ENST00000398117.1:c.586-24636A>G	ENSP00000381185.1:n.586-24636A>G
ENST00000590515.1:n.24+8451A>G
NM_000633.2:c.586-24636A>G	NP_000624.2:n.586-24636A>G
XR_935246.1:n.2026-24636A>G
XR_935248.1:n.1805-24636A>G
XR_935248.3:n.2307-24636A>G
NM_000633.3:c.586-24636A>G MANE Select	NP_000624.2:n.586-24636A>G