HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189563768T>C , CM000664.2:g.189563768T>C | GRCh38 |
NC_000002.11:g.190428494T>C , CM000664.1:g.190428494T>C | GRCh37 |
NC_000002.10:g.190136739T>C | NCBI36 |
NG_009027.1:g.22044A>G , LRG_837:g.22044A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261024.7:c.1218A>G MANE Select | ENSP00000261024.3:p.Glu406= | |
ENST00000261024.6:c.1218A>G | ENSP00000261024.2:p.Glu406= | |
NM_014585.5:c.1218A>G , LRG_837t1:c.1218A>G | NP_055400.1:p.Glu406= | |
XM_005246505.1:c.1098A>G | XP_005246562.1:p.Glu366= | |
XM_005246505.2:c.1098A>G | XP_005246562.1:p.Glu366= | |
XM_017003938.2:c.1098A>G | XP_016859427.1:p.Glu366= | |
NM_014585.6:c.1218A>G MANE Select | NP_055400.1:p.Glu406= |