HGVS | Genome Assembly |
---|---|
NC_000021.9:g.34370675C>G , CM000683.2:g.34370675C>G | GRCh38 |
NC_000021.8:g.35742974C>G , CM000683.1:g.35742974C>G | GRCh37 |
NC_000021.7:g.34664844C>G | NCBI36 |
NG_008804.1:g.11652C>G , LRG_291:g.11652C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000290310.4:c.197C>G MANE Select | ENSP00000290310.2:p.Ala66Gly | |
ENST00000290310.3:c.197C>G | ENSP00000290310.2:p.Ala66Gly | |
NM_172201.1:c.197C>G , LRG_291t1:c.197C>G | NP_751951.1:p.Ala66Gly | |
XR_937683.1:n.646G>C | ||
XR_937684.1:n.646G>C | ||
XR_001755012.2:n.767G>C | ||
XR_001755013.2:n.646G>C | ||
XR_937683.2:n.646G>C | ||
NM_172201.2:c.197C>G MANE Select | NP_751951.1:p.Ala66Gly |