Canonical Allele Identifier: CA2397714899

Gene: BCR

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23285276G= , CM000684.2:g.23285276G=	GRCh38
NC_000022.10:g.23627463G= , CM000684.1:g.23627463G=	GRCh37
NC_000022.9:g.21957463G=	NCBI36
NG_009244.1:g.109912G=
NG_009244.2:g.109912G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.2406+75G= MANE Select	ENSP00000303507.8:n.2406+75G=
ENST00000305877.12:c.2406+75G=	ENSP00000303507.8:n.2406+75G=
ENST00000359540.7:c.2406+75G=	ENSP00000352535.3:n.2406+75G=
ENST00000398512.9:c.1270-2868G=	ENSP00000381524.6:n.1270-2868G=
ENST00000466076.1:n.480+75G=
ENST00000487968.5:n.1059+75G=
NM_004327.3:c.2406+75G=	NP_004318.3:n.2406+75G=
NM_021574.2:c.2406+75G=	NP_067585.2:n.2406+75G=
XR_001755448.1:n.1062C=
NM_004327.4:c.2406+75G= MANE Select	NP_004318.3:n.2406+75G=
NM_021574.3:c.2406+75G=	NP_067585.2:n.2406+75G=