HGVS | Genome Assembly |
---|---|
NC_000005.10:g.44388450_44388451delinsCG , CM000667.2:g.44388450_44388451delinsCG | GRCh38 |
NC_000005.9:g.44388552_44388553delinsCG , CM000667.1:g.44388552_44388553delinsCG | GRCh37 |
NC_000005.8:g.44424309_44424310delinsCG | NCBI36 |
NG_011446.1:g.5232_5233delinsCG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264664.5:c.232_233delinsCG MANE Select | ENSP00000264664.4:p.Arg78= | |
ENST00000264664.4:c.232_233delinsCG | ENSP00000264664.4:p.Arg78= | |
NM_004465.1:c.232_233delinsCG | NP_004456.1:p.Arg78= | |
XM_005248264.2:c.232_233delinsCG | XP_005248321.1:p.Arg78= | |
XM_005248264.4:c.232_233delinsCG | XP_005248321.1:p.Arg78= | |
NM_004465.2:c.232_233delinsCG MANE Select | NP_004456.1:p.Arg78= |