HGVS | Genome Assembly |
---|---|
NC_000022.11:g.29312962G= , CM000684.2:g.29312962G= | GRCh38 |
NC_000022.10:g.29708951G= , CM000684.1:g.29708951G= | GRCh37 |
NC_000022.9:g.28038951G= | NCBI36 |
NG_032959.1:g.10956G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000216101.7:c.*339C= MANE Select | ENSP00000216101.6:n.*339C= | |
ENST00000216101.6:c.*339C= | ENSP00000216101.6:n.*339C= | |
ENST00000401450.3:c.*897C= | ENSP00000386095.3:n.*897C= | |
NM_006477.4:c.*339C= | NP_006468.1:n.*339C= | |
XM_011529821.1:c.*339C= | XP_011528123.1:n.*339C= | |
XM_011529822.1:c.*339C= | XP_011528124.1:n.*339C= | |
XM_011529823.1:c.*339C= | XP_011528125.1:n.*339C= | |
NM_006477.5:c.*339C= MANE Select | NP_006468.1:n.*339C= |