HGVS | Genome Assembly |
---|---|
NC_000001.11:g.153796866C>T , CM000663.2:g.153796866C>T | GRCh38 |
NC_000001.10:g.153769342C>T , CM000663.1:g.153769342C>T | GRCh37 |
NC_000001.9:g.152035966C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000637918.1:c.136-6790G>A | ||
ENST00000427283.1:n.819+301C>T | ||
XM_017003084.2:c.53+303C>T | XP_016858573.1:n.53+303C>T | |
XM_017003085.2:c.53+303C>T | XP_016858574.1:n.53+303C>T |