HGVS | Genome Assembly |
---|---|
NC_000021.9:g.43774295T= , CM000683.2:g.43774295T= | GRCh38 |
NC_000021.8:g.45194176T= , CM000683.1:g.45194176T= | GRCh37 |
NC_000021.7:g.44018604T= | NCBI36 |
NG_011545.1:g.7084A= , LRG_485:g.7084A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291568.7:c.204A= MANE Select | ENSP00000291568.6:p.Arg68= | |
ENST00000480147.3:n.1974A= | ||
ENST00000639959.1:c.71A= | ||
ENST00000640406.1:c.*279A= | ENSP00000492672.1:n.*279A= | |
ENST00000675996.1:n.629A= | ||
ENST00000291568.5:c.204A= | ENSP00000291568.5:p.Arg68= | |
ENST00000480147.1:n.568A= | ||
NM_000100.3:c.204A= , LRG_485t1:c.204A= | NP_000091.1:p.Arg68= | |
NM_000100.4:c.204A= MANE Select | NP_000091.1:p.Arg68= |