HGVS | Genome Assembly |
---|---|
NC_000019.10:g.35285018G= , CM000681.2:g.35285018G= | GRCh38 |
NC_000019.9:g.35775921G= , CM000681.1:g.35775921G= | GRCh37 |
NC_000019.8:g.40467761G= | NCBI36 |
NG_011563.1:g.7512G= | |
NG_011563.2:g.7512G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000222304.5:c.231G= MANE Select | ENSP00000222304.2:p.Lys77= | |
ENST00000222304.3:c.231G= | ENSP00000222304.2:p.Lys77= | |
ENST00000593580.1:n.2502G= | ||
ENST00000598398.5:c.231G= | ENSP00000471894.1:p.Lys77= | |
NM_021175.2:c.231G= | NP_066998.1:p.Lys77= | |
NM_021175.3:c.231G= | NP_066998.1:p.Lys77= | |
NM_021175.4:c.231G= MANE Select | NP_066998.1:p.Lys77= |