HGVS | Genome Assembly |
---|---|
NC_000006.12:g.139373052C= , CM000668.2:g.139373052C= | GRCh38 |
NC_000006.11:g.139694189C= , CM000668.1:g.139694189C= | GRCh37 |
NC_000006.10:g.139735882C= | NCBI36 |
NG_016169.1:g.6597G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367651.4:c.*80G= MANE Select | ENSP00000356623.2:n.*80G= | |
ENST00000367651.3:c.*80G= | ENSP00000356623.2:n.*80G= | |
ENST00000536159.2:c.*80G= | ENSP00000442831.1:n.*80G= | |
ENST00000537332.2:c.*80G= | ENSP00000444198.2:n.*80G= | |
NM_001168388.2:c.*80G= | NP_001161860.1:n.*80G= | |
NM_001168389.2:c.*80G= | NP_001161861.2:n.*80G= | |
NM_006079.4:c.*80G= | NP_006070.2:n.*80G= | |
NM_006079.5:c.*80G= MANE Select | NP_006070.2:n.*80G= | |
NM_001168388.3:c.*80G= | NP_001161860.1:n.*80G= | |
NM_001168389.3:c.*80G= | NP_001161861.2:n.*80G= |