HGVS | Genome Assembly |
---|---|
NC_000022.11:g.42126115T>C , CM000684.2:g.42126115T>C | GRCh38 |
NC_000022.10:g.42522120T>C , CM000684.1:g.42522120T>C | GRCh37 |
NC_000022.9:g.40852064T>C | NCBI36 |
NG_008376.3:g.8877A>G | |
NG_008376.4:g.9696A>G |
HGVS | Amino-acid Change | |
---|---|---|
XM_011529966.1:c.1453-162A>G | XP_011528268.1:n.1453-162A>G | |
XM_011529967.1:c.1453-162A>G | XP_011528269.1:n.1453-162A>G | |
XM_011529968.1:c.1453-188A>G | XP_011528270.1:n.1453-188A>G | |
XM_011529969.1:c.1309-162A>G | XP_011528271.1:n.1309-162A>G | |
XM_011529970.1:c.1300-162A>G | XP_011528272.1:n.1300-162A>G |