HGVS | Genome Assembly |
---|---|
NC_000016.10:g.81357870G>A , CM000678.2:g.81357870G>A | GRCh38 |
NC_000016.9:g.81391475G>A , CM000678.1:g.81391475G>A | GRCh37 |
NC_000016.8:g.79948976G>A | NCBI36 |
NG_009007.1:g.47905G>A , LRG_242:g.47905G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000648349.2:c.*620G>A | ENSP00000498114.1:n.*620G>A | |
ENST00000648994.2:c.912G>A MANE Select | ENSP00000497351.1:p.Gln304= | |
ENST00000650388.1:c.446G>A | ENSP00000498081.1:n.446G>A | |
ENST00000568107.2:c.912G>A | ENSP00000476795.1:p.Gln304= | |
NM_022041.3:c.912G>A , LRG_242t1:c.912G>A | NP_071324.1:p.Gln304= | |
XM_017023734.1:c.273G>A | XP_016879223.1:p.Gln91= | |
NM_001377486.1:c.273G>A | NP_001364415.1:p.Gln91= | |
NM_022041.4:c.912G>A MANE Select | NP_071324.1:p.Gln304= |