HGVS | Genome Assembly |
---|---|
NC_000002.12:g.73640829A= , CM000664.2:g.73640829A= | GRCh38 |
NC_000002.11:g.73867956A= , CM000664.1:g.73867956A= | GRCh37 |
NC_000002.10:g.73721464A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000272425.4:c.*116T= MANE Select | ENSP00000272425.3:n.*116T= | |
NM_003960.3:c.*116T= | NP_003951.3:n.*116T= | |
NM_003960.4:c.*116T= MANE Select | NP_003951.3:n.*116T= |