HGVS | Genome Assembly |
---|---|
NC_000019.10:g.15640751T>C , CM000681.2:g.15640751T>C | GRCh38 |
NC_000019.9:g.15751561T>C , CM000681.1:g.15751561T>C | GRCh37 |
NC_000019.8:g.15612561T>C | NCBI36 |
NG_007964.1:g.4855T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000620621.4:c.344-6301T>C | ENSP00000478605.1:n.344-6301T>C |