Canonical Allele Identifier: CA2397726913

Gene: BCR

Linked Data

• dbSNP Id: rs2073976591

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23308839dup , CM000684.2:g.23308839dup	GRCh38
NC_000022.10:g.23651026dup , CM000684.1:g.23651026dup	GRCh37
NC_000022.9:g.21981026dup	NCBI36
NG_009244.1:g.133475dup
NG_009244.2:g.133475dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.3013-585dup MANE Select	ENSP00000303507.8:n.3013-585dup
ENST00000305877.12:c.3013-585dup	ENSP00000303507.8:n.3013-585dup
ENST00000359540.7:c.2881-585dup	ENSP00000352535.3:n.2881-585dup
ENST00000398512.9:c.1709-585dup	ENSP00000381524.6:n.1709-585dup
ENST00000419722.6:n.238-585dup
ENST00000475025.5:n.87-585dup
ENST00000478978.5:n.294-585dup
NM_004327.3:c.3013-585dup	NP_004318.3:n.3013-585dup
NM_021574.2:c.2881-585dup	NP_067585.2:n.2881-585dup
NM_004327.4:c.3013-585dup MANE Select	NP_004318.3:n.3013-585dup
NM_021574.3:c.2881-585dup	NP_067585.2:n.2881-585dup