HGVS | Genome Assembly |
---|---|
NC_000011.10:g.22625057A= , CM000673.2:g.22625057A= | GRCh38 |
NC_000011.9:g.22646603A= , CM000673.1:g.22646603A= | GRCh37 |
NC_000011.8:g.22603179A= | NCBI36 |
NG_007425.1:g.5785T= , LRG_527:g.5785T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327470.6:c.754T= MANE Select | ENSP00000330875.3:p.Cys252= | |
ENST00000327470.4:c.754T= | ENSP00000330875.3:p.Cys252= | |
NM_022725.3:c.754T= , LRG_527t1:c.754T= | NP_073562.1:p.Cys252= | |
NM_022725.4:c.754T= MANE Select | NP_073562.1:p.Cys252= |