HGVS | Genome Assembly |
---|---|
NC_000017.11:g.5002589T>G , CM000679.2:g.5002589T>G | GRCh38 |
NC_000017.10:g.4905884T>G , CM000679.1:g.4905884T>G | GRCh37 |
NC_000017.9:g.4846608T>G | NCBI36 |
NG_034137.1:g.9642T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320785.10:c.555T>G (KIF1C) MANE Select | ENSP00000320821.5:p.Ala185= | |
ENST00000320785.9:c.555T>G (KIF1C) | ENSP00000320821.5:p.Ala185= | |
NM_006612.5:c.555T>G (KIF1C) | NP_006603.2:p.Ala185= | |
XM_005256424.1:c.555T>G (KIF1C) | XP_005256481.1:p.Ala185= | |
XM_005256424.2:c.555T>G (KIF1C) | XP_005256481.1:p.Ala185= | |
XM_024450745.1:c.-39+3493A>C (INCA1) | XP_024306513.1:n.-39+3493A>C | |
NM_006612.6:c.555T>G (KIF1C) MANE Select | NP_006603.2:p.Ala185= |