HGVS | Genome Assembly |
---|---|
NC_000004.12:g.73404283T= , CM000666.2:g.73404283T= | GRCh38 |
NC_000004.11:g.74270000T= , CM000666.1:g.74270000T= | GRCh37 |
NC_000004.10:g.74488864T= | NCBI36 |
NG_009291.1:g.5029T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295897.8:c.-45T= | ENSP00000295897.4:n.-45T= | |
ENST00000441319.5:c.48-86T= | ENSP00000392541.1:n.48-86T= | |
ENST00000621628.4:c.-45T= | ENSP00000480485.1:n.-45T= | |
NM_000477.5:c.-45T= | NP_000468.1:n.-45T= | |
NM_000477.6:c.-45T= | NP_000468.1:n.-45T= |