HGVS | Genome Assembly |
---|---|
NC_000015.10:g.26774455C>T , CM000677.2:g.26774455C>T | GRCh38 |
NC_000015.9:g.27019602C>T , CM000677.1:g.27019602C>T | GRCh37 |
NC_000015.8:g.24570695C>T | NCBI36 |
NG_012836.1:g.4326G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000541819.6:c.249-1683G>A | ENSP00000442408.2:n.249-1683G>A | |
ENST00000557641.5:n.453-1683G>A |