HGVS | Genome Assembly |
---|---|
NC_000024.10:g.19589561T>G , CM000686.2:g.19589561T>G | GRCh38 |
NC_000024.9:g.21751447T>G , CM000686.1:g.21751447T>G | GRCh37 |
NC_000024.8:g.20210835T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000686158.1:n.538T>G | ||
ENST00000686905.1:n.1623T>G | ||
ENST00000693214.1:n.1711T>G | ||
ENST00000445715.6:n.440T>G | ||
ENST00000407724.7:n.784T>G | ||
ENST00000445715.5:n.440T>G | ||
ENST00000447202.2:n.2475T>G | ||
ENST00000447520.5:n.440T>G | ||
ENST00000459719.6:n.1711T>G | ||
ENST00000538014.2:n.1730T>G | ||
ENST00000585549.5:n.83T>G | ||
ENST00000587095.1:n.81T>G | ||
ENST00000588613.5:n.149T>G | ||
ENST00000589075.5:n.122T>G | ||
NR_045128.1:n.464T>G | ||
NR_045129.1:n.464T>G |