HGVS | Genome Assembly |
---|---|
NC_000010.11:g.124749442A>T , CM000672.2:g.124749442A>T | GRCh38 |
NC_000010.10:g.126438011A>T , CM000672.1:g.126438011A>T | GRCh37 |
NC_000010.9:g.126428001A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000494792.1:c.628+10944T>A | ||
ENST00000495711.2:c.187-956T>A |