HGVS | Genome Assembly |
---|---|
NC_000017.11:g.5002546A>T , CM000679.2:g.5002546A>T | GRCh38 |
NC_000017.10:g.4905841A>T , CM000679.1:g.4905841A>T | GRCh37 |
NC_000017.9:g.4846565A>T | NCBI36 |
NG_034137.1:g.9599A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320785.10:c.512A>T (KIF1C) MANE Select | ENSP00000320821.5:p.His171Leu | |
ENST00000320785.9:c.512A>T (KIF1C) | ENSP00000320821.5:p.His171Leu | |
NM_006612.5:c.512A>T (KIF1C) | NP_006603.2:p.His171Leu | |
XM_005256424.1:c.512A>T (KIF1C) | XP_005256481.1:p.His171Leu | |
XM_005256424.2:c.512A>T (KIF1C) | XP_005256481.1:p.His171Leu | |
XM_024450745.1:c.-39+3536T>A (INCA1) | XP_024306513.1:n.-39+3536T>A | |
NM_006612.6:c.512A>T (KIF1C) MANE Select | NP_006603.2:p.His171Leu |