HGVS | Genome Assembly |
---|---|
NC_000017.11:g.8086034C>T , CM000679.2:g.8086034C>T | GRCh38 |
NC_000017.10:g.7989352C>T , CM000679.1:g.7989352C>T | GRCh37 |
NC_000017.9:g.7930077C>T | NCBI36 |
NG_007099.1:g.6670G>A | |
NG_007099.2:g.6683G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647874.1:c.334G>A MANE Select | ENSP00000497784.1:p.Ala112Thr | |
ENST00000319144.4:c.334G>A | ENSP00000315167.4:p.Ala112Thr | |
NM_001139.2:c.334G>A | NP_001130.1:p.Ala112Thr | |
NM_001139.3:c.334G>A MANE Select | NP_001130.1:p.Ala112Thr |