HGVS | Genome Assembly |
---|---|
NC_000016.10:g.23301864G= , CM000678.2:g.23301864G= | GRCh38 |
NC_000016.9:g.23313185G= , CM000678.1:g.23313185G= | GRCh37 |
NC_000016.8:g.23220686G= | NCBI36 |
NG_011908.1:g.4595G= |
HGVS | Amino-acid Change |
---|---|
ENST00000569789.1:n.178+18060G= | |
XM_017023525.1:c.49+18060G= | XP_016879014.1:n.49+18060G= |
XM_017023526.1:c.49+18060G= | XP_016879015.1:n.49+18060G= |