HGVS | Genome Assembly |
---|---|
NC_000017.11:g.47733359C>A , CM000679.2:g.47733359C>A | GRCh38 |
NC_000017.10:g.45810725C>A , CM000679.1:g.45810725C>A | GRCh37 |
NC_000017.9:g.43165724C>A | NCBI36 |
NG_012166.1:g.5116C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000177694.2:c.-96C>A MANE Select | ENSP00000177694.1:n.-96C>A | |
ENST00000177694.1:c.-96C>A | ENSP00000177694.1:n.-96C>A | |
NM_013351.1:c.-96C>A | NP_037483.1:n.-96C>A | |
XM_011524698.1:c.-96C>A | XP_011523000.1:n.-96C>A | |
NM_013351.2:c.-96C>A MANE Select | NP_037483.1:n.-96C>A |