Canonical Allele Identifier: CA5045368

Gene: CD72

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35615952C>T , CM000671.2:g.35615952C>T	GRCh38
NC_000009.11:g.35615949C>T , CM000671.1:g.35615949C>T	GRCh37
NC_000009.10:g.35605949C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259633.9:c.679G>A MANE Select	ENSP00000259633.4:p.Gly227Ser
ENST00000259633.8:c.679G>A	ENSP00000259633.4:p.Gly227Ser
ENST00000396757.5:c.679G>A	ENSP00000379980.1:p.Gly227Ser
ENST00000463720.5:n.787G>A
ENST00000477364.5:n.681G>A
ENST00000490239.5:n.1060G>A
ENST00000612238.4:c.679G>A	ENSP00000483742.1:p.Gly227Ser
NM_001782.2:c.679G>A	NP_001773.1:p.Gly227Ser
XM_006716893.1:c.679G>A	XP_006716956.1:p.Gly227Ser
XM_006716894.2:c.667G>A	XP_006716957.1:p.Gly223Ser
XM_011518074.1:c.667G>A	XP_011516376.1:p.Gly223Ser
XM_006716893.2:c.679G>A	XP_006716956.1:p.Gly227Ser
NM_001782.3:c.679G>A MANE Select	NP_001773.1:p.Gly227Ser