HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41583142T= , CM000679.2:g.41583142T= | GRCh38 |
NC_000017.10:g.39739394T= , CM000679.1:g.39739394T= | GRCh37 |
NC_000017.9:g.36992920T= | NCBI36 |
NG_008624.1:g.8754A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.1275-2A= MANE Select | ENSP00000167586.6:n.1275-2A= | |
ENST00000167586.6:c.1275-2A= | ENSP00000167586.6:n.1275-2A= | |
ENST00000441550.2:n.222-2A= | ||
NM_000526.4:c.1275-2A= | NP_000517.2:n.1275-2A= | |
NM_000526.5:c.1275-2A= MANE Select | NP_000517.3:n.1275-2A= |