Canonical Allele Identifier: CA5045380
Gene: CD72 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35616047G>A , CM000671.2:g.35616047G>A GRCh38
NC_000009.11:g.35616044G>A , CM000671.1:g.35616044G>A GRCh37
NC_000009.10:g.35606044G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000259633.9:c.584C>T MANE Select ENSP00000259633.4:p.Thr195Met
ENST00000259633.8:c.584C>T ENSP00000259633.4:p.Thr195Met
ENST00000396757.5:c.584C>T ENSP00000379980.1:p.Thr195Met
ENST00000463720.5:n.692C>T
ENST00000477364.5:n.586C>T
ENST00000490239.5:n.965C>T
ENST00000612238.4:c.584C>T ENSP00000483742.1:p.Thr195Met
NM_001782.2:c.584C>T NP_001773.1:p.Thr195Met
XM_006716893.1:c.584C>T XP_006716956.1:p.Thr195Met
XM_006716894.2:c.572C>T XP_006716957.1:p.Thr191Met
XM_011518074.1:c.572C>T XP_011516376.1:p.Thr191Met
XM_006716893.2:c.584C>T XP_006716956.1:p.Thr195Met
NM_001782.3:c.584C>T MANE Select NP_001773.1:p.Thr195Met