HGVS | Genome Assembly |
---|---|
NC_000020.11:g.10658465T= , CM000682.2:g.10658465T= | GRCh38 |
NC_000020.10:g.10639113T= , CM000682.1:g.10639113T= | GRCh37 |
NC_000020.9:g.10587113T= | NCBI36 |
NG_007496.1:g.20582A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000254958.10:c.694+3A= MANE Select | ENSP00000254958.4:n.694+3A= | |
ENST00000254958.9:c.694+3A= | ENSP00000254958.4:n.694+3A= | |
ENST00000423891.6:n.560+3A= | ||
NM_000214.2:c.694+3A= | NP_000205.1:n.694+3A= | |
NM_000214.3:c.694+3A= MANE Select | NP_000205.1:n.694+3A= |