HGVS | Genome Assembly |
---|---|
NC_000002.12:g.73640859T>A , CM000664.2:g.73640859T>A | GRCh38 |
NC_000002.11:g.73867986T>A , CM000664.1:g.73867986T>A | GRCh37 |
NC_000002.10:g.73721494T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000272425.4:c.*86A>T MANE Select | ENSP00000272425.3:n.*86A>T | |
ENST00000272425.3:c.*86A>T | ENSP00000272425.3:n.*86A>T | |
NM_003960.3:c.*86A>T | NP_003951.3:n.*86A>T | |
NM_003960.4:c.*86A>T MANE Select | NP_003951.3:n.*86A>T |