Canonical Allele Identifier: CA2397674404

Gene: BCR

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23203806A= , CM000684.2:g.23203806A=	GRCh38
NC_000022.10:g.23545993A= , CM000684.1:g.23545993A=	GRCh37
NC_000022.9:g.21875993A=	NCBI36
NG_009244.1:g.28442A=
NG_009244.2:g.28442A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000305877.13:c.1279+21567A= MANE Select	ENSP00000303507.8:n.1279+21567A=
ENST00000305877.12:c.1279+21567A=	ENSP00000303507.8:n.1279+21567A=
ENST00000359540.7:c.1279+21567A=	ENSP00000352535.3:n.1279+21567A=
ENST00000398512.9:c.1269+21577A=	ENSP00000381524.6:n.1269+21577A=
ENST00000463770.5:n.133+5421A=
ENST00000479188.5:n.129+23974A=
ENST00000487679.1:n.196+4454A=
NM_004327.3:c.1279+21567A=	NP_004318.3:n.1279+21567A=
NM_021574.2:c.1279+21567A=	NP_067585.2:n.1279+21567A=
NM_004327.4:c.1279+21567A= MANE Select	NP_004318.3:n.1279+21567A=
NM_021574.3:c.1279+21567A=	NP_067585.2:n.1279+21567A=