HGVS | Genome Assembly |
---|---|
NC_000013.11:g.28659102G= , CM000675.2:g.28659102G= | GRCh38 |
NC_000013.10:g.29233239G= , CM000675.1:g.29233239G= | GRCh37 |
NC_000013.9:g.28131239G= | NCBI36 |
NG_027550.1:g.5099G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000697716.1:c.-168G= | ENSP00000513414.1:n.-168G= | |
NM_015932.5:c.-83G= | NP_057016.1:n.-83G= |