Canonical Allele Identifier: CA400603662

Gene: CD79B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63929439A>G , CM000679.2:g.63929439A>G	GRCh38
NC_000017.10:g.62006799A>G , CM000679.1:g.62006799A>G	GRCh37
NC_000017.9:g.59360531A>G	NCBI36
NG_007368.1:g.7906T>C , LRG_43:g.7906T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000626.4:c.586T>C MANE Select	NP_000617.1:p.Tyr196His
ENST00000006750.8:c.586T>C MANE Select	ENSP00000006750.4:p.Tyr196His
NM_000626.2:c.586T>C	NP_000617.1:p.Tyr196His
NM_000626.3:c.586T>C	NP_000617.1:p.Tyr196His
NM_001039933.1:c.589T>C , LRG_43t1:c.589T>C	NP_001035022.1:p.Tyr197His
NM_001039933.2:c.589T>C	NP_001035022.1:p.Tyr197His
NM_001039933.3:c.589T>C	NP_001035022.1:p.Tyr197His
NM_001329050.1:c.277T>C	NP_001315979.1:p.Tyr93His
NM_001329050.2:c.277T>C	NP_001315979.1:p.Tyr93His
NM_021602.2:c.274T>C	NP_067613.1:p.Tyr92His
NM_021602.3:c.274T>C	NP_067613.1:p.Tyr92His
NM_021602.4:c.274T>C	NP_067613.1:p.Tyr92His
ENST00000006750.7:c.586T>C	ENSP00000006750.3:p.Tyr196His
ENST00000349817.2:c.274T>C	ENSP00000245862.2:p.Tyr92His
ENST00000392795.7:c.589T>C	ENSP00000376544.3:p.Tyr197His
ENST00000559358.1:n.597T>C
ENST00000647774.1:c.207T>C
ENST00000698624.1:n.583T>C
XM_005257858.3:c.277T>C	XP_005257915.1:p.Tyr93His