Canonical Allele Identifier: CA301800428

Gene: BCL2

Linked Data

• dbSNP Id: rs993956744
• MyVariant Identifiers: chr18:g.60986167G>A (hg19) ; chr18:g.63318934G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318934G>A , CM000680.2:g.63318934G>A	GRCh38
NC_000018.9:g.60986167G>A , CM000680.1:g.60986167G>A	GRCh37
NC_000018.8:g.59137147G>A	NCBI36
NG_009361.1:g.5447C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-268C>T MANE Select	ENSP00000329623.3:n.-268C>T
ENST00000333681.4:c.-268C>T	ENSP00000329623.3:n.-268C>T
ENST00000398117.1:c.-268C>T	ENSP00000381185.1:n.-268C>T
NM_000633.2:c.-268C>T	NP_000624.2:n.-268C>T
NM_000657.2:c.-268C>T	NP_000648.2:n.-268C>T
XM_011526135.1:c.-268C>T	XP_011524437.1:n.-268C>T
XR_935246.1:n.845C>T
XR_935247.1:n.845C>T
XR_935248.1:n.624C>T
XM_011526135.3:c.-268C>T	XP_011524437.1:n.-268C>T
XM_017025917.2:c.-268C>T	XP_016881406.1:n.-268C>T
XR_935248.3:n.1126C>T
NM_000633.3:c.-268C>T MANE Select	NP_000624.2:n.-268C>T
NM_000657.3:c.-268C>T	NP_000648.2:n.-268C>T