Canonical Allele Identifier: CA406036569
Gene: CD79A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41879607T>C , CM000681.2:g.41879607T>C GRCh38
NC_000019.9:g.42383677T>C , CM000681.1:g.42383677T>C GRCh37
NC_000019.8:g.47075517T>C NCBI36
NG_009619.1:g.7488T>C , LRG_42:g.7488T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000597454.2:c.697T>C ENSP00000468922.2:p.Ser233Pro
ENST00000221972.8:c.452T>C MANE Select ENSP00000221972.3:p.Ile151Thr
ENST00000221972.7:c.452T>C ENSP00000221972.3:p.Ile151Thr
ENST00000444740.2:c.338T>C ENSP00000400605.1:p.Ile113Thr
ENST00000597454.1:c.697T>C ENSP00000468922.1:p.Ser233Pro
NM_001783.3:c.452T>C , LRG_42t1:c.452T>C NP_001774.1:p.Ile151Thr
NM_021601.3:c.338T>C NP_067612.1:p.Ile113Thr
NM_001783.4:c.452T>C MANE Select NP_001774.1:p.Ile151Thr
NM_021601.4:c.338T>C NP_067612.1:p.Ile113Thr