Canonical Allele Identifier: CA301779637

Gene: BCL2

Linked Data

• dbSNP Id: rs991538288
• gnomAD v3: 18-63291394-C-T
• gnomAD v4: 18-63291394-C-T
• MyVariant Identifiers: chr18:g.60958627C>T (hg19) ; chr18:g.63291394C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63291394C>T , CM000680.2:g.63291394C>T	GRCh38
NC_000018.9:g.60958627C>T , CM000680.1:g.60958627C>T	GRCh37
NC_000018.8:g.59109607C>T	NCBI36
NG_009361.1:g.32987G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000333681.5:c.585+26688G>A MANE Select	ENSP00000329623.3:n.585+26688G>A
ENST00000677227.1:c.586-10180G>A	ENSP00000504566.1:n.586-10180G>A
ENST00000678134.1:c.789+10268G>A	ENSP00000503628.1:n.789+10268G>A
ENST00000678349.1:c.1137+26136G>A	ENSP00000504190.1:n.1137+26136G>A
ENST00000333681.4:c.585+26688G>A	ENSP00000329623.3:n.585+26688G>A
ENST00000398117.1:c.585+26688G>A	ENSP00000381185.1:n.585+26688G>A
NM_000633.2:c.585+26688G>A	NP_000624.2:n.585+26688G>A
XR_935246.1:n.1698-10180G>A
XR_935247.1:n.1698-10180G>A
XR_935248.1:n.1477-10180G>A
XR_935248.3:n.1979-10180G>A
NM_000633.3:c.585+26688G>A MANE Select	NP_000624.2:n.585+26688G>A