HGVS | Genome Assembly |
---|---|
NC_000021.9:g.34370652A>C , CM000683.2:g.34370652A>C | GRCh38 |
NC_000021.8:g.35742951A>C , CM000683.1:g.35742951A>C | GRCh37 |
NC_000021.7:g.34664821A>C | NCBI36 |
NG_008804.1:g.11629A>C , LRG_291:g.11629A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000290310.4:c.174A>C MANE Select | ENSP00000290310.2:p.Gly58= | |
ENST00000290310.3:c.174A>C | ENSP00000290310.2:p.Gly58= | |
NM_172201.1:c.174A>C , LRG_291t1:c.174A>C | NP_751951.1:p.Gly58= | |
XR_937683.1:n.669T>G | ||
XR_937684.1:n.669T>G | ||
XR_001755012.2:n.790T>G | ||
XR_001755013.2:n.669T>G | ||
XR_937683.2:n.669T>G | ||
NM_172201.2:c.174A>C MANE Select | NP_751951.1:p.Gly58= |