HGVS | Genome Assembly |
---|---|
NC_000004.12:g.68670433A>G , CM000666.2:g.68670433A>G | GRCh38 |
NC_000004.11:g.69536151A>G , CM000666.1:g.69536151A>G | GRCh37 |
NC_000004.10:g.69218746A>G | NCBI36 |
NG_052676.1:g.5344T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000338206.6:c.186T>C MANE Select | ENSP00000341045.5:p.Thr62= | |
ENST00000338206.5:c.186T>C | ENSP00000341045.5:p.Thr62= | |
ENST00000616841.4:c.186T>C | ENSP00000482004.1:p.Thr62= | |
NM_001076.3:c.186T>C | NP_001067.2:p.Thr62= | |
NM_001076.4:c.186T>C MANE Select | NP_001067.2:p.Thr62= |