HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189005332T= , CM000664.2:g.189005332T= | GRCh38 |
NC_000002.11:g.189870058T= , CM000664.1:g.189870058T= | GRCh37 |
NC_000002.10:g.189578303T= | NCBI36 |
NG_007404.1:g.35960T= , LRG_3:g.35960T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000450867.2:c.2833-18T= | ENSP00000415346.2:n.2833-18T= | |
ENST00000304636.9:c.2932-18T= MANE Select | ENSP00000304408.4:n.2932-18T= | |
ENST00000304636.7:c.2932-18T= | ENSP00000304408.3:n.2932-18T= | |
ENST00000317840.9:c.2527+2296T= | ENSP00000315243.6:n.2527+2296T= | |
NM_000090.3:c.2932-18T= , LRG_3t1:c.2932-18T= | NP_000081.1:n.2932-18T= | |
NM_000090.4:c.2932-18T= MANE Select | NP_000081.2:n.2932-18T= |