HGVS | Genome Assembly |
---|---|
NC_000006.12:g.151526760C>T , CM000668.2:g.151526760C>T | GRCh38 |
NC_000006.11:g.151847895C>T , CM000668.1:g.151847895C>T | GRCh37 |
NC_000006.10:g.151889588C>T | NCBI36 |
NG_021198.1:g.37721C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000239374.8:c.58-9558C>T MANE Select | ENSP00000239374.6:n.58-9558C>T | |
ENST00000239374.7:c.58-9558C>T | ENSP00000239374.6:n.58-9558C>T | |
NM_025059.3:c.58-9558C>T | NP_079335.2:n.58-9558C>T | |
NM_025059.4:c.58-9558C>T MANE Select | NP_079335.2:n.58-9558C>T |