HGVS | Genome Assembly |
---|---|
NC_000021.9:g.34370668A= , CM000683.2:g.34370668A= | GRCh38 |
NC_000021.8:g.35742967A= , CM000683.1:g.35742967A= | GRCh37 |
NC_000021.7:g.34664837A= | NCBI36 |
NG_008804.1:g.11645A= , LRG_291:g.11645A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000290310.4:c.190A= MANE Select | ENSP00000290310.2:p.Ile64= | |
ENST00000290310.3:c.190A= | ENSP00000290310.2:p.Ile64= | |
NM_172201.1:c.190A= , LRG_291t1:c.190A= | NP_751951.1:p.Ile64= | |
XR_937683.1:n.653T= | ||
XR_937684.1:n.653T= | ||
XR_001755012.2:n.774T= | ||
XR_001755013.2:n.653T= | ||
XR_937683.2:n.653T= | ||
NM_172201.2:c.190A= MANE Select | NP_751951.1:p.Ile64= |