HGVS | Genome Assembly |
---|---|
NC_000021.9:g.34370672T= , CM000683.2:g.34370672T= | GRCh38 |
NC_000021.8:g.35742971T= , CM000683.1:g.35742971T= | GRCh37 |
NC_000021.7:g.34664841T= | NCBI36 |
NG_008804.1:g.11649T= , LRG_291:g.11649T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000290310.4:c.194T= MANE Select | ENSP00000290310.2:p.Val65= | |
ENST00000290310.3:c.194T= | ENSP00000290310.2:p.Val65= | |
NM_172201.1:c.194T= , LRG_291t1:c.194T= | NP_751951.1:p.Val65= | |
XR_937683.1:n.649A= | ||
XR_937684.1:n.649A= | ||
XR_001755012.2:n.770A= | ||
XR_001755013.2:n.649A= | ||
XR_937683.2:n.649A= | ||
NM_172201.2:c.194T= MANE Select | NP_751951.1:p.Val65= |