HGVS | Genome Assembly |
---|---|
NC_000010.11:g.133538771T= , CM000672.2:g.133538771T= | GRCh38 |
NC_000010.10:g.135352275T= , CM000672.1:g.135352275T= | GRCh37 |
NC_000010.9:g.135202265T= | NCBI36 |
NG_008383.1:g.16409T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252945.8:c.1298-9T= MANE Select | ENSP00000252945.3:n.1298-9T= | |
ENST00000252945.7:c.1298-9T= | ENSP00000252945.3:n.1298-9T= | |
ENST00000368520.1:n.1358+879T= | ||
ENST00000418356.1:c.887-9T= | ENSP00000397299.1:n.887-9T= | |
ENST00000421586.5:c.1037-9T= | ENSP00000412754.1:n.1037-9T= | |
ENST00000463117.6:c.1298-9T= | ENSP00000440689.1:n.1298-9T= | |
ENST00000469258.1:n.394-9T= | ||
ENST00000541080.5:c.714-9T= | ||
NM_000773.3:c.1298-9T= | NP_000764.1:n.1298-9T= | |
NM_000773.4:c.1298-9T= MANE Select | NP_000764.1:n.1298-9T= |