HGVS | Genome Assembly |
---|---|
NC_000021.9:g.34370572G>A , CM000683.2:g.34370572G>A | GRCh38 |
NC_000021.8:g.35742871G>A , CM000683.1:g.35742871G>A | GRCh37 |
NC_000021.7:g.34664741G>A | NCBI36 |
NG_008804.1:g.11549G>A , LRG_291:g.11549G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000290310.4:c.94G>A MANE Select | ENSP00000290310.2:p.Ala32Thr | |
ENST00000290310.3:c.94G>A | ENSP00000290310.2:p.Ala32Thr | |
NM_172201.1:c.94G>A , LRG_291t1:c.94G>A | NP_751951.1:p.Ala32Thr | |
XR_937683.1:n.749C>T | ||
XR_937684.1:n.749C>T | ||
XR_001755012.2:n.870C>T | ||
XR_001755013.2:n.749C>T | ||
XR_937683.2:n.749C>T | ||
NM_172201.2:c.94G>A MANE Select | NP_751951.1:p.Ala32Thr |