Canonical Allele Identifier: CA2397726861
Gene: BCR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23308759G= , CM000684.2:g.23308759G= GRCh38
NC_000022.10:g.23650946G= , CM000684.1:g.23650946G= GRCh37
NC_000022.9:g.21980946G= NCBI36
NG_009244.1:g.133395G=
NG_009244.2:g.133395G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305877.13:c.3013-665G= MANE Select ENSP00000303507.8:n.3013-665G=
ENST00000305877.12:c.3013-665G= ENSP00000303507.8:n.3013-665G=
ENST00000359540.7:c.2881-665G= ENSP00000352535.3:n.2881-665G=
ENST00000398512.9:c.1709-665G= ENSP00000381524.6:n.1709-665G=
ENST00000419722.6:n.238-665G=
ENST00000475025.5:n.87-665G=
ENST00000478978.5:n.294-665G=
NM_004327.3:c.3013-665G= NP_004318.3:n.3013-665G=
NM_021574.2:c.2881-665G= NP_067585.2:n.2881-665G=
NM_004327.4:c.3013-665G= MANE Select NP_004318.3:n.3013-665G=
NM_021574.3:c.2881-665G= NP_067585.2:n.2881-665G=