HGVS | Genome Assembly |
---|---|
NC_000001.11:g.170074763G>T , CM000663.2:g.170074763G>T | GRCh38 |
NC_000001.10:g.170043904G>T , CM000663.1:g.170043904G>T | GRCh37 |
NC_000001.9:g.168310528G>T | NCBI36 |
NG_012883.2:g.4976C>A | |
NG_012883.3:g.4976C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000490550.1:n.174+10272C>A | ||
XM_024454186.1:c.77+10272C>A | XP_024309954.1:n.77+10272C>A | |
XM_024454187.1:c.77+10272C>A | XP_024309955.1:n.77+10272C>A |