Canonical Allele Identifier: CA2308706791
Gene: BCL2 HGNC NCBI

Linked Data

dbSNP Id: rs1912640468

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63291355T>G , CM000680.2:g.63291355T>G GRCh38
NC_000018.9:g.60958588T>G , CM000680.1:g.60958588T>G GRCh37
NC_000018.8:g.59109568T>G NCBI36
NG_009361.1:g.33026A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000333681.5:c.585+26727A>C MANE Select ENSP00000329623.3:n.585+26727A>C
ENST00000677227.1:c.586-10141A>C ENSP00000504566.1:n.586-10141A>C
ENST00000678134.1:c.789+10307A>C ENSP00000503628.1:n.789+10307A>C
ENST00000678349.1:c.1137+26175A>C ENSP00000504190.1:n.1137+26175A>C
ENST00000333681.4:c.585+26727A>C ENSP00000329623.3:n.585+26727A>C
ENST00000398117.1:c.585+26727A>C ENSP00000381185.1:n.585+26727A>C
NM_000633.2:c.585+26727A>C NP_000624.2:n.585+26727A>C
XR_935246.1:n.1698-10141A>C
XR_935247.1:n.1698-10141A>C
XR_935248.1:n.1477-10141A>C
XR_935248.3:n.1979-10141A>C
NM_000633.3:c.585+26727A>C MANE Select NP_000624.2:n.585+26727A>C