HGVS | Genome Assembly |
---|---|
NC_000021.9:g.34370870G>A , CM000683.2:g.34370870G>A | GRCh38 |
NC_000021.8:g.35743169G>A , CM000683.1:g.35743169G>A | GRCh37 |
NC_000021.7:g.34665039G>A | NCBI36 |
NG_008804.1:g.11847G>A , LRG_291:g.11847G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000290310.4:c.*20G>A MANE Select | ENSP00000290310.2:n.*20G>A | |
ENST00000290310.3:c.*20G>A | ENSP00000290310.2:n.*20G>A | |
NM_172201.1:c.*20G>A , LRG_291t1:c.*20G>A | NP_751951.1:n.*20G>A | |
XR_937683.1:n.451C>T | ||
XR_937684.1:n.451C>T | ||
XR_001755012.2:n.572C>T | ||
XR_001755013.2:n.451C>T | ||
XR_937683.2:n.451C>T | ||
NM_172201.2:c.*20G>A MANE Select | NP_751951.1:n.*20G>A |