HGVS | Genome Assembly |
---|---|
NC_000011.10:g.22625029G= , CM000673.2:g.22625029G= | GRCh38 |
NC_000011.9:g.22646575G= , CM000673.1:g.22646575G= | GRCh37 |
NC_000011.8:g.22603151G= | NCBI36 |
NG_007425.1:g.5813C= , LRG_527:g.5813C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327470.6:c.782C= MANE Select | ENSP00000330875.3:p.Thr261= | |
ENST00000327470.4:c.782C= | ENSP00000330875.3:p.Thr261= | |
NM_022725.3:c.782C= , LRG_527t1:c.782C= | NP_073562.1:p.Thr261= | |
NM_022725.4:c.782C= MANE Select | NP_073562.1:p.Thr261= |