HGVS | Genome Assembly |
---|---|
NC_000004.12:g.24794775T>C , CM000666.2:g.24794775T>C | GRCh38 |
NC_000004.11:g.24796397T>C , CM000666.1:g.24796397T>C | GRCh37 |
NC_000004.10:g.24405495T>C | NCBI36 |
NG_012213.1:g.4313T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000598411.1:c.-17+4673T>C | ENSP00000472134.1:n.-17+4673T>C |