HGVS | Genome Assembly |
---|---|
NC_000004.12:g.73404224T= , CM000666.2:g.73404224T= | GRCh38 |
NC_000004.11:g.74269941T= , CM000666.1:g.74269941T= | GRCh37 |
NC_000004.10:g.74488805T= | NCBI36 |
NG_009291.1:g.4970T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000441319.5:c.48-145T= | ENSP00000392541.1:n.48-145T= |