HGVS | Genome Assembly |
---|---|
NC_000015.10:g.26774621A>G , CM000677.2:g.26774621A>G | GRCh38 |
NC_000015.9:g.27019768A>G , CM000677.1:g.27019768A>G | GRCh37 |
NC_000015.8:g.24570861A>G | NCBI36 |
NG_012836.1:g.4160T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000541819.6:c.249-1849T>C | ENSP00000442408.2:n.249-1849T>C | |
ENST00000557641.5:n.453-1849T>C |