Canonical Allele Identifier: CA2397726862
Gene: BCR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23308760G= , CM000684.2:g.23308760G= GRCh38
NC_000022.10:g.23650947G= , CM000684.1:g.23650947G= GRCh37
NC_000022.9:g.21980947G= NCBI36
NG_009244.1:g.133396G=
NG_009244.2:g.133396G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305877.13:c.3013-664G= MANE Select ENSP00000303507.8:n.3013-664G=
ENST00000305877.12:c.3013-664G= ENSP00000303507.8:n.3013-664G=
ENST00000359540.7:c.2881-664G= ENSP00000352535.3:n.2881-664G=
ENST00000398512.9:c.1709-664G= ENSP00000381524.6:n.1709-664G=
ENST00000419722.6:n.238-664G=
ENST00000475025.5:n.87-664G=
ENST00000478978.5:n.294-664G=
NM_004327.3:c.3013-664G= NP_004318.3:n.3013-664G=
NM_021574.2:c.2881-664G= NP_067585.2:n.2881-664G=
NM_004327.4:c.3013-664G= MANE Select NP_004318.3:n.3013-664G=
NM_021574.3:c.2881-664G= NP_067585.2:n.2881-664G=