HGVS | Genome Assembly |
---|---|
NC_000021.9:g.31923801A>G , CM000683.2:g.31923801A>G | GRCh38 |
NC_000021.8:g.33296113A>G , CM000683.1:g.33296113A>G | GRCh37 |
NC_000021.7:g.32217984A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270112.7:c.262-667A>G MANE Select | ENSP00000270112.2:n.262-667A>G | |
ENST00000270112.6:c.262-667A>G | ENSP00000270112.2:n.262-667A>G | |
NM_014586.1:c.262-667A>G | NP_055401.1:n.262-667A>G | |
XM_011529537.1:c.262-667A>G | XP_011527839.1:n.262-667A>G | |
XM_011529537.2:c.262-667A>G | XP_011527839.1:n.262-667A>G | |
NM_014586.2:c.262-667A>G MANE Select | NP_055401.1:n.262-667A>G |