HGVS | Genome Assembly |
---|---|
NC_000006.12:g.151526733T>C , CM000668.2:g.151526733T>C | GRCh38 |
NC_000006.11:g.151847868T>C , CM000668.1:g.151847868T>C | GRCh37 |
NC_000006.10:g.151889561T>C | NCBI36 |
NG_021198.1:g.37694T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000239374.8:c.58-9585T>C MANE Select | ENSP00000239374.6:n.58-9585T>C | |
ENST00000239374.7:c.58-9585T>C | ENSP00000239374.6:n.58-9585T>C | |
NM_025059.3:c.58-9585T>C | NP_079335.2:n.58-9585T>C | |
NM_025059.4:c.58-9585T>C MANE Select | NP_079335.2:n.58-9585T>C |