HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42998749A= , CM000679.2:g.42998749A= | GRCh38 |
NC_000017.10:g.41150766A= , CM000679.1:g.41150766A= | GRCh37 |
NC_000017.9:g.38404292A= | NCBI36 |
NG_053099.1:g.5477A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000253788.12:c.-2A= MANE Select | ENSP00000253788.5:n.-2A= | |
ENST00000589913.6:c.-2A= | ENSP00000464813.1:n.-2A= | |
ENST00000590864.2:c.-2A= | ENSP00000467939.2:n.-2A= | |
ENST00000253788.9:c.-2A= | ENSP00000253788.4:n.-2A= | |
ENST00000587478.1:n.54A= | ||
ENST00000588830.1:c.-2A= | ENSP00000468468.1:n.-2A= | |
ENST00000589037.5:c.-2A= | ENSP00000467587.1:n.-2A= | |
ENST00000589913.5:c.-2A= | ENSP00000464813.1:n.-2A= | |
ENST00000593262.1:n.331A= | ||
NM_000988.3:c.-2A= | NP_000979.1:n.-2A= | |
NM_000988.5:c.-2A= MANE Select | NP_000979.1:n.-2A= | |
NM_001349921.1:c.-2A= | NP_001336850.1:n.-2A= | |
NM_001349922.1:c.-2A= | NP_001336851.1:n.-2A= | |
NR_146327.1:n.82A= | ||
NM_001349921.2:c.-2A= | NP_001336850.1:n.-2A= | |
NM_001349922.2:c.-2A= | NP_001336851.1:n.-2A= | |
NR_146327.2:n.54A= |