HGVS | Genome Assembly |
---|---|
NC_000017.11:g.16949021A= , CM000679.2:g.16949021A= | GRCh38 |
NC_000017.10:g.16852335A= , CM000679.1:g.16852335A= | GRCh37 |
NC_000017.9:g.16793060A= | NCBI36 |
NG_007281.1:g.28068T= , LRG_120:g.28068T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261652.7:c.200-38T= MANE Select | ENSP00000261652.2:n.200-38T= | |
ENST00000261652.6:c.200-38T= | ENSP00000261652.2:n.200-38T= | |
ENST00000579315.5:c.200-38T= | ENSP00000464069.1:n.200-38T= | |
ENST00000581616.2:n.203-38T= | ||
ENST00000582931.5:n.104-38T= | ||
ENST00000583789.1:c.62-38T= | ENSP00000462952.1:n.62-38T= | |
ENST00000584950.5:c.62-38T= | ENSP00000463582.1:n.62-38T= | |
NM_012452.2:c.200-38T= , LRG_120t1:c.200-38T= | NP_036584.1:n.200-38T= | |
NM_012452.3:c.200-38T= MANE Select | NP_036584.1:n.200-38T= |