HGVS | Genome Assembly |
---|---|
NC_000014.9:g.60509892C>T , CM000676.2:g.60509892C>T | GRCh38 |
NC_000014.8:g.60976610C>T , CM000676.1:g.60976610C>T | GRCh37 |
NC_000014.7:g.60046363C>T | NCBI36 |
NG_008203.1:g.5673C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000327720.6:c.494C>T (SIX6) MANE Select | ENSP00000328596.5:p.Thr165Ile | |
ENST00000327720.5:c.494C>T (SIX6) | ENSP00000328596.5:p.Thr165Ile | |
ENST00000556799.1:c.-144+5503G>A (C14orf39) | ENSP00000451441.1:n.-144+5503G>A | |
NM_007374.2:c.494C>T (SIX6) | NP_031400.2:p.Thr165Ile | |
NM_007374.3:c.494C>T (SIX6) MANE Select | NP_031400.2:p.Thr165Ile |