HGVS | Genome Assembly |
---|---|
NC_000021.9:g.43417088G>A , CM000683.2:g.43417088G>A | GRCh38 |
NG_052009.1:g.15045C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270162.8:c.2006C>T MANE Select | ENSP00000270162.6:p.Ala669Val | |
ENST00000270162.6:c.2006C>T | ENSP00000270162.6:p.Ala669Val | |
NM_173354.3:c.2006C>T | NP_775490.2:p.Ala669Val | |
XM_011529474.1:c.1859C>T | XP_011527776.1:p.Ala620Val | |
NM_173354.4:c.2006C>T | NP_775490.2:p.Ala669Val | |
XM_011529474.2:c.1859C>T | XP_011527776.1:p.Ala620Val | |
NM_173354.5:c.2006C>T MANE Select | NP_775490.2:p.Ala669Val |