HGVS | Genome Assembly |
---|---|
NC_000019.10:g.48703912T>C , CM000681.2:g.48703912T>C | GRCh38 |
NC_000019.9:g.49207169T>C , CM000681.1:g.49207169T>C | GRCh37 |
NC_000019.8:g.53898981T>C | NCBI36 |
NG_007511.1:g.12942T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000425340.3:c.956T>C MANE Select | ENSP00000387498.2:p.Ile319Thr | |
ENST00000522966.2:c.956T>C | ENSP00000430227.2:p.Ile319Thr | |
ENST00000391876.5:c.956T>C | ENSP00000375748.4:p.Ile319Thr | |
ENST00000425340.2:c.956T>C | ENSP00000387498.2:p.Ile319Thr | |
NM_000511.5:c.956T>C | NP_000502.4:p.Ile319Thr | |
NM_001097638.2:c.956T>C | NP_001091107.1:p.Ile319Thr | |
NM_000511.6:c.956T>C MANE Select | NP_000502.4:p.Ile319Thr | |
NM_001097638.3:c.956T>C | NP_001091107.1:p.Ile319Thr |