Canonical Allele Identifier: CA157918
Gene: CD79A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41879574C>A , CM000681.2:g.41879574C>A GRCh38
NC_000019.9:g.42383644C>A , CM000681.1:g.42383644C>A GRCh37
NC_000019.8:g.47075484C>A NCBI36
NG_009619.1:g.7455C>A , LRG_42:g.7455C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000597454.2:c.664C>A ENSP00000468922.2:p.Pro222Thr
ENST00000221972.8:c.419C>A MANE Select ENSP00000221972.3:p.Thr140Asn
ENST00000221972.7:c.419C>A ENSP00000221972.3:p.Thr140Asn
ENST00000444740.2:c.305C>A ENSP00000400605.1:p.Thr102Asn
ENST00000597454.1:c.664C>A ENSP00000468922.1:p.Pro222Thr
NM_001783.3:c.419C>A , LRG_42t1:c.419C>A NP_001774.1:p.Thr140Asn
NM_021601.3:c.305C>A NP_067612.1:p.Thr102Asn
NM_001783.4:c.419C>A MANE Select NP_001774.1:p.Thr140Asn
NM_021601.4:c.305C>A NP_067612.1:p.Thr102Asn