HGVS | Genome Assembly |
---|---|
NC_000021.9:g.43416990G= , CM000683.2:g.43416990G= | GRCh38 |
NG_052009.1:g.15143C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270162.8:c.2104C= MANE Select | ENSP00000270162.6:p.Leu702= | |
ENST00000270162.6:c.2104C= | ENSP00000270162.6:p.Leu702= | |
NM_173354.3:c.2104C= | NP_775490.2:p.Leu702= | |
XM_011529474.1:c.1957C= | XP_011527776.1:p.Leu653= | |
NM_173354.4:c.2104C= | NP_775490.2:p.Leu702= | |
XM_011529474.2:c.1957C= | XP_011527776.1:p.Leu653= | |
NM_173354.5:c.2104C= MANE Select | NP_775490.2:p.Leu702= |