HGVS | Genome Assembly |
---|---|
NC_000020.11:g.46011596T= , CM000682.2:g.46011596T= | GRCh38 |
NC_000020.10:g.44640235T= , CM000682.1:g.44640235T= | GRCh37 |
NC_000020.9:g.44073642T= | NCBI36 |
NG_011468.1:g.7689T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000372330.3:c.846T= MANE Select | ENSP00000361405.3:p.Asn282= | |
NM_004994.2:c.846T= | NP_004985.2:p.Asn282= | |
NM_004994.3:c.846T= MANE Select | NP_004985.2:p.Asn282= |