HGVS | Genome Assembly |
---|---|
NC_000011.10:g.14076987C>T , CM000673.2:g.14076987C>T | GRCh38 |
NC_000011.9:g.14098534C>T , CM000673.1:g.14098534C>T | GRCh37 |
NC_000011.8:g.14055110C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000576479.4:c.553+1569C>T MANE Select | ENSP00000460236.1:n.553+1569C>T | |
ENST00000576479.3:c.553+1569C>T | ENSP00000460236.1:n.553+1569C>T | |
NM_006108.3:c.553+1569C>T | NP_006099.2:n.553+1569C>T | |
NM_006108.4:c.553+1569C>T MANE Select | NP_006099.2:n.553+1569C>T |