Canonical Allele Identifier: CA2270155001

Gene: CD79B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63928899G= , CM000679.2:g.63928899G=	GRCh38
NC_000017.10:g.62006259G= , CM000679.1:g.62006259G=	GRCh37
NC_000017.9:g.59359991G=	NCBI36
NG_007368.1:g.8446C= , LRG_43:g.8446C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000626.4:c.*327C= MANE Select	NP_000617.1:n.*327C=
ENST00000006750.8:c.*327C= MANE Select	ENSP00000006750.4:n.*327C=
NM_000626.2:c.*327C=	NP_000617.1:n.*327C=
NM_000626.3:c.*327C=	NP_000617.1:n.*327C=
NM_001039933.1:c.*327C= , LRG_43t1:c.*327C=	NP_001035022.1:n.*327C=
NM_001039933.2:c.*327C=	NP_001035022.1:n.*327C=
NM_001039933.3:c.*327C=	NP_001035022.1:n.*327C=
NM_001329050.1:c.*327C=	NP_001315979.1:n.*327C=
NM_001329050.2:c.*327C=	NP_001315979.1:n.*327C=
NM_021602.2:c.*327C=	NP_067613.1:n.*327C=
NM_021602.3:c.*327C=	NP_067613.1:n.*327C=
NM_021602.4:c.*327C=	NP_067613.1:n.*327C=
ENST00000006750.7:c.*327C=	ENSP00000006750.3:n.*327C=
ENST00000392795.7:c.*327C=	ENSP00000376544.3:n.*327C=
ENST00000559358.1:n.1028C=
ENST00000647774.1:c.288+350C=
ENST00000698624.1:n.1014C=
XM_005257858.3:c.*327C=	XP_005257915.1:n.*327C=