HGVS | Genome Assembly |
---|---|
NC_000019.10:g.1106785T= , CM000681.2:g.1106785T= | GRCh38 |
NC_000019.9:g.1106784T= , CM000681.1:g.1106784T= | GRCh37 |
NC_000019.8:g.1057784T= | NCBI36 |
NG_050621.1:g.7860T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000354171.12:c.*213T= | ENSP00000346103.7:n.*213T= | |
ENST00000588919.5:c.*19T= | ENSP00000464989.3:n.*19T= | |
ENST00000592940.2:n.1178T= | ||
ENST00000616066.4:c.*213T= | ENSP00000485000.1:n.*213T= | |
ENST00000622390.4:c.*213T= | ENSP00000477503.1:n.*213T= | |
NM_001039847.2:c.*145T= | NP_001034936.1:n.*145T= | |
NM_001039848.2:c.*213T= | NP_001034937.1:n.*213T= | |
NM_002085.4:c.*213T= | NP_002076.2:n.*213T= | |
NM_001039848.3:c.*213T= | NP_001034937.1:n.*213T= |