HGVS | Genome Assembly |
---|---|
NC_000005.10:g.151822635G= , CM000667.2:g.151822635G= | GRCh38 |
NC_000005.9:g.151202196G= , CM000667.1:g.151202196G= | GRCh37 |
NC_000005.8:g.151182389G= | NCBI36 |
NG_011764.1:g.107202C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000274576.9:c.*38C= MANE Select | ENSP00000274576.5:n.*38C= | |
ENST00000274576.8:c.*38C= | ENSP00000274576.4:n.*38C= | |
ENST00000455880.2:c.*38C= | ENSP00000411593.2:n.*38C= | |
ENST00000462581.6:c.*1146C= | ENSP00000430595.1:n.*1146C= | |
NM_000171.3:c.*38C= | NP_000162.2:n.*38C= | |
NM_001146040.1:c.*38C= | NP_001139512.1:n.*38C= | |
NM_001292000.1:c.*38C= | NP_001278929.1:n.*38C= | |
NM_000171.4:c.*38C= MANE Select | NP_000162.2:n.*38C= | |
NM_001146040.2:c.*38C= | NP_001139512.1:n.*38C= | |
NM_001292000.2:c.*38C= | NP_001278929.1:n.*38C= |