HGVS | Genome Assembly |
---|---|
NC_000001.11:g.155290568C= , CM000663.2:g.155290568C= | GRCh38 |
NC_000001.10:g.155260359C= , CM000663.1:g.155260359C= | GRCh37 |
NC_000001.9:g.153526983C= | NCBI36 |
NG_011677.1:g.15867G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000342741.6:c.*4G= MANE Select | ENSP00000339933.4:n.*4G= | |
ENST00000342741.4:c.*4G= | ENSP00000339933.4:n.*4G= | |
ENST00000392414.7:c.*4G= | ENSP00000376214.3:n.*4G= | |
NM_000298.5:c.*4G= | NP_000289.1:n.*4G= | |
NM_181871.3:c.*4G= | NP_870986.1:n.*4G= | |
XM_005245266.3:c.*4G= | XP_005245323.1:n.*4G= | |
XM_006711386.2:c.*4G= | XP_006711449.1:n.*4G= | |
XM_011509640.1:c.*4G= | XP_011507942.1:n.*4G= | |
NM_000298.6:c.*4G= MANE Select | NP_000289.1:n.*4G= | |
XM_006711386.4:c.*4G= | XP_006711449.1:n.*4G= | |
XM_011509640.3:c.*4G= | XP_011507942.1:n.*4G= | |
NM_181871.4:c.*4G= | NP_870986.1:n.*4G= |