HGVS | Genome Assembly |
---|---|
NC_000021.9:g.43416845G>A , CM000683.2:g.43416845G>A | GRCh38 |
NG_052009.1:g.15288C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270162.8:c.2249C>T MANE Select | ENSP00000270162.6:p.Ala750Val | |
ENST00000270162.6:c.2249C>T | ENSP00000270162.6:p.Ala750Val | |
NM_173354.3:c.2249C>T | NP_775490.2:p.Ala750Val | |
XM_011529474.1:c.2102C>T | XP_011527776.1:p.Ala701Val | |
NM_173354.4:c.2249C>T | NP_775490.2:p.Ala750Val | |
XM_011529474.2:c.2102C>T | XP_011527776.1:p.Ala701Val | |
NM_173354.5:c.2249C>T MANE Select | NP_775490.2:p.Ala750Val |