HGVS | Genome Assembly |
---|---|
NC_000008.11:g.81478702A= , CM000670.2:g.81478702A= | GRCh38 |
NC_000008.10:g.82390937A= , CM000670.1:g.82390937A= | GRCh37 |
NC_000008.9:g.82553492A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256104.5:c.*163T= MANE Select | ENSP00000256104.4:n.*163T= | |
ENST00000256104.4:c.*163T= | ENSP00000256104.4:n.*163T= | |
ENST00000518669.5:n.497T= | ||
ENST00000522659.1:c.*438T= | ENSP00000428385.1:n.*438T= | |
NM_001442.2:c.*163T= | NP_001433.1:n.*163T= | |
XR_001745980.1:n.514+16728A= | ||
NM_001442.3:c.*163T= MANE Select | NP_001433.1:n.*163T= |