HGVS | Genome Assembly |
---|---|
NC_000020.11:g.8885071C>T , CM000682.2:g.8885071C>T | GRCh38 |
NC_000020.10:g.8865718C>T , CM000682.1:g.8865718C>T | GRCh37 |
NC_000020.9:g.8813718C>T | NCBI36 |
NG_028168.1:g.757423C>T |
HGVS | Amino-acid Change |
---|---|
ENST00000487210.5:c.2764-77125C>T | |
ENST00000635929.1:c.593-77125C>T |