HGVS | Genome Assembly |
---|---|
NC_000010.11:g.102503788T>C , CM000672.2:g.102503788T>C | GRCh38 |
NC_000010.10:g.104263545T>C , CM000672.1:g.104263545T>C | GRCh37 |
NC_000010.9:g.104253535T>C | NCBI36 |
NG_011901.1:g.3968A>G | |
NG_021338.1:g.4827T>C , LRG_521:g.4827T>C |
HGVS | Amino-acid Change | |
---|---|---|
XM_011539859.1:c.-29-336T>C | XP_011538161.1:n.-29-336T>C | |
XM_011539863.1:c.8+802T>C | XP_011538165.1:n.8+802T>C | |
XM_011539863.3:c.8+802T>C | XP_011538165.1:n.8+802T>C |