HGVS | Genome Assembly |
---|---|
NC_000002.12:g.73640807C>A , CM000664.2:g.73640807C>A | GRCh38 |
NC_000002.11:g.73867934C>A , CM000664.1:g.73867934C>A | GRCh37 |
NC_000002.10:g.73721442C>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000272425.4:c.*138G>T MANE Select | ENSP00000272425.3:n.*138G>T | |
NM_003960.3:c.*138G>T | NP_003951.3:n.*138G>T | |
NM_003960.4:c.*138G>T MANE Select | NP_003951.3:n.*138G>T |