Canonical Allele Identifier: CA14408156
Gene: CD79B HGNC NCBI

Linked Data

dbSNP Id: rs7921

Genomic Alleles

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

Transcript Alleles

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