HGVS | Genome Assembly |
---|---|
NC_000008.11:g.16992922T= , CM000670.2:g.16992922T= | GRCh38 |
NC_000008.10:g.16850431T= , CM000670.1:g.16850431T= | GRCh37 |
NC_000008.9:g.16894802T= | NCBI36 |
NG_015978.1:g.14244A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000180166.6:c.*150A= MANE Select | ENSP00000180166.5:n.*150A= | |
ENST00000180166.5:c.*150A= | ENSP00000180166.5:n.*150A= | |
NM_019851.2:c.*150A= | NP_062825.1:n.*150A= | |
NM_019851.3:c.*150A= MANE Select | NP_062825.1:n.*150A= |