HGVS | Genome Assembly |
---|---|
NC_000017.11:g.70179302T= , CM000679.2:g.70179302T= | GRCh38 |
NC_000017.10:g.68175443T= , CM000679.1:g.68175443T= | GRCh37 |
NC_000017.9:g.65687038T= | NCBI36 |
NG_008798.1:g.14768T= , LRG_328:g.14768T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000243457.4:c.*2979T= MANE Select | ENSP00000243457.2:n.*2979T= | |
ENST00000243457.3:c.*2979T= | ENSP00000243457.2:n.*2979T= | |
NM_000891.2:c.*2979T= , LRG_328t1:c.*2979T= | NP_000882.1:n.*2979T= | |
NM_000891.3:c.*2979T= MANE Select | NP_000882.1:n.*2979T= |