HGVS | Genome Assembly |
---|---|
NC_000010.11:g.92419077T>C , CM000672.2:g.92419077T>C | GRCh38 |
NC_000010.10:g.94178834T>C , CM000672.1:g.94178834T>C | GRCh37 |
NC_000010.9:g.94168814T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000430958.1:n.411T>C | ||
NR_038243.2:n.417T>C |