HGVS | Genome Assembly |
---|---|
NC_000006.12:g.28161816A>C , CM000668.2:g.28161816A>C | GRCh38 |
NC_000006.11:g.28129594A>C , CM000668.1:g.28129594A>C | GRCh37 |
NC_000006.10:g.28237573A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000562227.2:n.48A>C | ||
ENST00000440790.6:n.36A>C | ||
ENST00000570126.1:n.25A>C | ||
NR_103448.1:n.56A>C |