HGVS | Genome Assembly |
---|---|
NC_000013.11:g.28659065T= , CM000675.2:g.28659065T= | GRCh38 |
NC_000013.10:g.29233202T= , CM000675.1:g.29233202T= | GRCh37 |
NC_000013.9:g.28131202T= | NCBI36 |
NG_027550.1:g.5062T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000697716.1:c.-205T= | ENSP00000513414.1:n.-205T= | |
NM_015932.5:c.-120T= | NP_057016.1:n.-120T= |