HGVS | Genome Assembly |
---|---|
NC_000010.11:g.124749460T>C , CM000672.2:g.124749460T>C | GRCh38 |
NC_000010.10:g.126438029T>C , CM000672.1:g.126438029T>C | GRCh37 |
NC_000010.9:g.126428019T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000494792.1:c.628+10926A>G | ||
ENST00000495711.2:c.187-974A>G |