HGVS | Genome Assembly |
---|---|
NC_000007.14:g.30897429G>T , CM000669.2:g.30897429G>T | GRCh38 |
NC_000007.13:g.30937044G>T , CM000669.1:g.30937044G>T | GRCh37 |
NC_000007.12:g.30903569G>T | NCBI36 |
NG_007475.2:g.49036G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000509504.2:c.621+14436G>T |