HGVS | Genome Assembly |
---|---|
NC_000014.9:g.60509805A>C , CM000676.2:g.60509805A>C | GRCh38 |
NC_000014.8:g.60976523A>C , CM000676.1:g.60976523A>C | GRCh37 |
NC_000014.7:g.60046276A>C | NCBI36 |
NG_008203.1:g.5586A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000327720.6:c.407A>C (SIX6) MANE Select | ENSP00000328596.5:p.Lys136Thr | |
ENST00000327720.5:c.407A>C (SIX6) | ENSP00000328596.5:p.Lys136Thr | |
ENST00000556799.1:c.-144+5590T>G (C14orf39) | ENSP00000451441.1:n.-144+5590T>G | |
NM_007374.2:c.407A>C (SIX6) | NP_031400.2:p.Lys136Thr | |
NM_007374.3:c.407A>C (SIX6) MANE Select | NP_031400.2:p.Lys136Thr |