HGVS | Genome Assembly |
---|---|
NC_000001.11:g.153796863T>C , CM000663.2:g.153796863T>C | GRCh38 |
NC_000001.10:g.153769339T>C , CM000663.1:g.153769339T>C | GRCh37 |
NC_000001.9:g.152035963T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000637918.1:c.136-6787A>G | ||
ENST00000427283.1:n.819+298T>C | ||
XM_017003084.2:c.53+300T>C | XP_016858573.1:n.53+300T>C | |
XM_017003085.2:c.53+300T>C | XP_016858574.1:n.53+300T>C |