HGVS | Genome Assembly |
---|---|
NC_000024.10:g.19589603T= , CM000686.2:g.19589603T= | GRCh38 |
NC_000024.9:g.21751489T= , CM000686.1:g.21751489T= | GRCh37 |
NC_000024.8:g.20210877T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000686158.1:n.580T= | ||
ENST00000686905.1:n.1665T= | ||
ENST00000693214.1:n.1753T= | ||
ENST00000445715.6:n.482T= | ||
ENST00000407724.7:n.826T= | ||
ENST00000445715.5:n.482T= | ||
ENST00000447202.2:n.2517T= | ||
ENST00000447520.5:n.482T= | ||
ENST00000459719.6:n.1753T= | ||
ENST00000538014.2:n.1772T= | ||
ENST00000585549.5:n.125T= | ||
ENST00000587095.1:n.123T= | ||
ENST00000588613.5:n.191T= | ||
ENST00000589075.5:n.164T= | ||
NR_045128.1:n.506T= | ||
NR_045129.1:n.506T= |