Canonical Allele Identifier: CA2397714912

Gene: BCR

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23285306T= , CM000684.2:g.23285306T=	GRCh38
NC_000022.10:g.23627493T= , CM000684.1:g.23627493T=	GRCh37
NC_000022.9:g.21957493T=	NCBI36
NG_009244.1:g.109942T=
NG_009244.2:g.109942T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.2406+105T= MANE Select	ENSP00000303507.8:n.2406+105T=
ENST00000305877.12:c.2406+105T=	ENSP00000303507.8:n.2406+105T=
ENST00000359540.7:c.2406+105T=	ENSP00000352535.3:n.2406+105T=
ENST00000398512.9:c.1270-2838T=	ENSP00000381524.6:n.1270-2838T=
ENST00000466076.1:n.480+105T=
ENST00000487968.5:n.1059+105T=
NM_004327.3:c.2406+105T=	NP_004318.3:n.2406+105T=
NM_021574.2:c.2406+105T=	NP_067585.2:n.2406+105T=
XR_001755448.1:n.1032A=
NM_004327.4:c.2406+105T= MANE Select	NP_004318.3:n.2406+105T=
NM_021574.3:c.2406+105T=	NP_067585.2:n.2406+105T=