HGVS | Genome Assembly |
---|---|
NC_000011.10:g.22624922T= , CM000673.2:g.22624922T= | GRCh38 |
NC_000011.9:g.22646468T= , CM000673.1:g.22646468T= | GRCh37 |
NC_000011.8:g.22603044T= | NCBI36 |
NG_007425.1:g.5920A= , LRG_527:g.5920A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327470.6:c.889A= MANE Select | ENSP00000330875.3:p.Thr297= | |
ENST00000327470.4:c.889A= | ENSP00000330875.3:p.Thr297= | |
NM_022725.3:c.889A= , LRG_527t1:c.889A= | NP_073562.1:p.Thr297= | |
NM_022725.4:c.889A= MANE Select | NP_073562.1:p.Thr297= |