HGVS | Genome Assembly |
---|---|
NC_000017.11:g.35576192A= , CM000679.2:g.35576192A= | GRCh38 |
NC_000017.10:g.33903211A= , CM000679.1:g.33903211A= | GRCh37 |
NC_000017.9:g.30927324A= | NCBI36 |
NG_008447.1:g.7446T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000225873.9:c.681-11T= MANE Select | ENSP00000225873.3:n.681-11T= | |
ENST00000586663.2:c.681-11T= | ENSP00000466894.2:n.681-11T= | |
ENST00000225873.8:c.681-11T= | ENSP00000225873.3:n.681-11T= | |
ENST00000586663.1:c.681-11T= | ENSP00000466894.1:n.681-11T= | |
ENST00000613219.4:c.681-11T= | ENSP00000482609.1:n.681-11T= | |
NM_000286.2:c.681-11T= | NP_000277.1:n.681-11T= | |
NM_000286.3:c.681-11T= MANE Select | NP_000277.1:n.681-11T= |