HGVS | Genome Assembly |
---|---|
NC_000024.10:g.19589848A>C , CM000686.2:g.19589848A>C | GRCh38 |
NC_000024.9:g.21751734A>C , CM000686.1:g.21751734A>C | GRCh37 |
NC_000024.8:g.20211122A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000686158.1:n.590-235A>C | ||
ENST00000686905.1:n.1910A>C | ||
ENST00000693214.1:n.1998A>C | ||
ENST00000445715.6:n.491+236A>C | ||
ENST00000407724.7:n.836-235A>C | ||
ENST00000445715.5:n.492-235A>C | ||
ENST00000447520.5:n.492-235A>C | ||
ENST00000459719.6:n.1763-235A>C | ||
ENST00000538014.2:n.2017A>C | ||
ENST00000585549.5:n.134+236A>C | ||
ENST00000587095.1:n.132+236A>C | ||
ENST00000588613.5:n.200+236A>C | ||
ENST00000589075.5:n.174-235A>C | ||
NR_045128.1:n.515+236A>C | ||
NR_045129.1:n.516-235A>C |