Canonical Allele Identifier: CA781297016

Gene: BCL2

Linked Data

• dbSNP Id: rs1202684600
• MyVariant Identifiers: chr18:g.60958554T>G (hg19) ; chr18:g.63291321T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63291321T>G , CM000680.2:g.63291321T>G	GRCh38
NC_000018.9:g.60958554T>G , CM000680.1:g.60958554T>G	GRCh37
NC_000018.8:g.59109534T>G	NCBI36
NG_009361.1:g.33060A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000333681.5:c.585+26761A>C MANE Select	ENSP00000329623.3:n.585+26761A>C
ENST00000677227.1:c.586-10107A>C	ENSP00000504566.1:n.586-10107A>C
ENST00000678134.1:c.789+10341A>C	ENSP00000503628.1:n.789+10341A>C
ENST00000678349.1:c.1137+26209A>C	ENSP00000504190.1:n.1137+26209A>C
ENST00000333681.4:c.585+26761A>C	ENSP00000329623.3:n.585+26761A>C
ENST00000398117.1:c.585+26761A>C	ENSP00000381185.1:n.585+26761A>C
NM_000633.2:c.585+26761A>C	NP_000624.2:n.585+26761A>C
XR_935246.1:n.1698-10107A>C
XR_935247.1:n.1698-10107A>C
XR_935248.1:n.1477-10107A>C
XR_935248.3:n.1979-10107A>C
NM_000633.3:c.585+26761A>C MANE Select	NP_000624.2:n.585+26761A>C