Canonical Allele Identifier: CA14690397
Gene: BCL3 HGNC NCBI

Linked Data

dbSNP Id: rs8100239

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44749847T>A , CM000681.2:g.44749847T>A GRCh38
NC_000019.9:g.45253104T>A , CM000681.1:g.45253104T>A GRCh37
NC_000019.8:g.49944944T>A NCBI36
NG_052809.1:g.12227T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000164227.10:c.256+801T>A MANE Select ENSP00000164227.5:n.256+801T>A
ENST00000164227.9:c.256+801T>A ENSP00000164227.5:n.256+801T>A
ENST00000403534.7:n.425-1380T>A
NM_005178.4:c.256+801T>A NP_005169.2:n.256+801T>A
XM_011527197.1:c.256+801T>A XP_011525499.1:n.256+801T>A
XM_011527198.1:c.256+801T>A XP_011525500.1:n.256+801T>A
XM_011527199.1:c.256+801T>A XP_011525501.1:n.256+801T>A
XM_011527197.2:c.511+801T>A XP_011525499.2:n.511+801T>A
XM_011527198.3:c.922+801T>A XP_011525500.2:n.922+801T>A
XM_011527200.2:c.-291T>A XP_011525502.1:n.-291T>A
XM_017027109.1:c.137-1380T>A XP_016882598.1:n.137-1380T>A
XM_017027110.1:c.137-1380T>A XP_016882599.1:n.137-1380T>A
NM_005178.5:c.256+801T>A MANE Select NP_005169.2:n.256+801T>A