Canonical Allele Identifier: CA301779608

Gene: BCL2

Linked Data

• dbSNP Id: rs915008249
• MyVariant Identifiers: chr18:g.60958565G>A (hg19) ; chr18:g.63291332G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63291332G>A , CM000680.2:g.63291332G>A	GRCh38
NC_000018.9:g.60958565G>A , CM000680.1:g.60958565G>A	GRCh37
NC_000018.8:g.59109545G>A	NCBI36
NG_009361.1:g.33049C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000333681.5:c.585+26750C>T MANE Select	ENSP00000329623.3:n.585+26750C>T
ENST00000677227.1:c.586-10118C>T	ENSP00000504566.1:n.586-10118C>T
ENST00000678134.1:c.789+10330C>T	ENSP00000503628.1:n.789+10330C>T
ENST00000678349.1:c.1137+26198C>T	ENSP00000504190.1:n.1137+26198C>T
ENST00000333681.4:c.585+26750C>T	ENSP00000329623.3:n.585+26750C>T
ENST00000398117.1:c.585+26750C>T	ENSP00000381185.1:n.585+26750C>T
NM_000633.2:c.585+26750C>T	NP_000624.2:n.585+26750C>T
XR_935246.1:n.1698-10118C>T
XR_935247.1:n.1698-10118C>T
XR_935248.1:n.1477-10118C>T
XR_935248.3:n.1979-10118C>T
NM_000633.3:c.585+26750C>T MANE Select	NP_000624.2:n.585+26750C>T