HGVS | Genome Assembly |
---|---|
NC_000016.10:g.28506335A= , CM000678.2:g.28506335A= | GRCh38 |
NC_000016.9:g.28517656A= , CM000678.1:g.28517656A= | GRCh37 |
NC_000016.8:g.28425157A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000356897.1:c.31+446T= MANE Select | ENSP00000349365.1:n.31+446T= | |
ENST00000568075.1:c.-362-2285T= | ENSP00000455990.1:n.-362-2285T= | |
NM_145659.3:c.31+446T= MANE Select | NP_663634.2:n.31+446T= | |
XM_011545780.1:c.38-2285T= | XP_011544082.1:n.38-2285T= | |
XM_011545780.2:c.38-2285T= | XP_011544082.1:n.38-2285T= |