HGVS | Genome Assembly |
---|---|
NC_000001.11:g.153796869T>G , CM000663.2:g.153796869T>G | GRCh38 |
NC_000001.10:g.153769345T>G , CM000663.1:g.153769345T>G | GRCh37 |
NC_000001.9:g.152035969T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000637918.1:c.136-6793A>C | ||
ENST00000427283.1:n.819+304T>G | ||
XM_017003084.2:c.53+306T>G | XP_016858573.1:n.53+306T>G | |
XM_017003085.2:c.53+306T>G | XP_016858574.1:n.53+306T>G |