HGVS | Genome Assembly |
---|---|
NC_000019.10:g.39243620C= , CM000681.2:g.39243620C= | GRCh38 |
NC_000019.9:g.39734260C= , CM000681.1:g.39734260C= | GRCh37 |
NC_000019.8:g.44426100C= | NCBI36 |
NG_042193.1:g.6352G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000613087.5:c.*12G= | ENSP00000481633.1:n.*12G= | |
ENST00000413851.3:c.*12G= MANE Select | ENSP00000409000.2:n.*12G= | |
ENST00000413851.2:c.*12G= | ENSP00000409000.2:n.*12G= | |
ENST00000613087.4:c.*12G= | ENSP00000481633.1:n.*12G= | |
XM_005258765.3:c.*12G= | XP_005258822.1:n.*12G= | |
XM_011526757.1:c.*12G= | XP_011525059.1:n.*12G= | |
NM_001346937.1:c.615G= | NP_001333866.1:n.615G= | |
NM_172139.3:c.*12G= | NP_742151.2:n.*12G= | |
NM_172139.4:c.*12G= MANE Select | NP_742151.2:n.*12G= | |
NM_001346937.2:c.*12G= | NP_001333866.1:n.*12G= |