HGVS | Genome Assembly |
---|---|
NC_000001.11:g.68438118C>A , CM000663.2:g.68438118C>A | GRCh38 |
NC_000001.10:g.68903801C>A , CM000663.1:g.68903801C>A | GRCh37 |
NC_000001.9:g.68676389C>A | NCBI36 |
NG_008472.1:g.16842G>T | |
NG_008472.2:g.16842G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262340.6:c.1128+69G>T MANE Select | ENSP00000262340.5:n.1128+69G>T | |
ENST00000262340.5:c.1128+69G>T | ENSP00000262340.5:n.1128+69G>T | |
NM_000329.2:c.1128+69G>T | NP_000320.1:n.1128+69G>T | |
XM_017002027.1:c.852+69G>T | XP_016857516.1:n.852+69G>T | |
NM_000329.3:c.1128+69G>T MANE Select | NP_000320.1:n.1128+69G>T |