HGVS | Genome Assembly |
---|---|
NC_000017.11:g.70179321A= , CM000679.2:g.70179321A= | GRCh38 |
NC_000017.10:g.68175462A= , CM000679.1:g.68175462A= | GRCh37 |
NC_000017.9:g.65687057A= | NCBI36 |
NG_008798.1:g.14787A= , LRG_328:g.14787A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000243457.4:c.*2998A= MANE Select | ENSP00000243457.2:n.*2998A= | |
ENST00000243457.3:c.*2998A= | ENSP00000243457.2:n.*2998A= | |
NM_000891.2:c.*2998A= , LRG_328t1:c.*2998A= | NP_000882.1:n.*2998A= | |
NM_000891.3:c.*2998A= MANE Select | NP_000882.1:n.*2998A= |