HGVS | Genome Assembly |
---|---|
NC_000006.12:g.151526739T>G , CM000668.2:g.151526739T>G | GRCh38 |
NC_000006.11:g.151847874T>G , CM000668.1:g.151847874T>G | GRCh37 |
NC_000006.10:g.151889567T>G | NCBI36 |
NG_021198.1:g.37700T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000239374.8:c.58-9579T>G MANE Select | ENSP00000239374.6:n.58-9579T>G | |
ENST00000239374.7:c.58-9579T>G | ENSP00000239374.6:n.58-9579T>G | |
NM_025059.3:c.58-9579T>G | NP_079335.2:n.58-9579T>G | |
NM_025059.4:c.58-9579T>G MANE Select | NP_079335.2:n.58-9579T>G |