Canonical Allele Identifier: CA2270155578

Gene: CD79B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63930138A= , CM000679.2:g.63930138A=	GRCh38
NC_000017.10:g.62007498A= , CM000679.1:g.62007498A=	GRCh37
NC_000017.9:g.59361230A=	NCBI36
NG_007368.1:g.7207T= , LRG_43:g.7207T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000626.4:c.366T= MANE Select	NP_000617.1:p.Cys122=
ENST00000006750.8:c.366T= MANE Select	ENSP00000006750.4:p.Cys122=
NM_000626.2:c.366T=	NP_000617.1:p.Cys122=
NM_000626.3:c.366T=	NP_000617.1:p.Cys122=
NM_001039933.1:c.369T= , LRG_43t1:c.369T=	NP_001035022.1:p.Cys123=
NM_001039933.2:c.369T=	NP_001035022.1:p.Cys123=
NM_001039933.3:c.369T=	NP_001035022.1:p.Cys123=
NM_001329050.1:c.122-250T=	NP_001315979.1:n.122-250T=
NM_001329050.2:c.122-250T=	NP_001315979.1:n.122-250T=
NM_021602.2:c.119-250T=	NP_067613.1:n.119-250T=
NM_021602.3:c.119-250T=	NP_067613.1:n.119-250T=
NM_021602.4:c.119-250T=	NP_067613.1:n.119-250T=
ENST00000006750.7:c.366T=	ENSP00000006750.3:p.Cys122=
ENST00000349817.2:c.119-250T=	ENSP00000245862.2:n.119-250T=
ENST00000392795.7:c.369T=	ENSP00000376544.3:p.Cys123=
ENST00000559358.1:n.377T=
ENST00000647774.1:c.52-250T=
ENST00000698624.1:n.363T=
XM_005257858.3:c.122-250T=	XP_005257915.1:n.122-250T=