HGVS | Genome Assembly |
---|---|
NC_000022.11:g.42126222C= , CM000684.2:g.42126222C= | GRCh38 |
NC_000022.10:g.42522224C= , CM000684.1:g.42522224C= | GRCh37 |
NC_000022.9:g.40852168C= | NCBI36 |
NG_008376.3:g.8770G= | |
NG_008376.4:g.9589G= |
HGVS | Amino-acid Change | |
---|---|---|
XM_011529966.1:c.1453-269G= | XP_011528268.1:n.1453-269G= | |
XM_011529967.1:c.1453-269G= | XP_011528269.1:n.1453-269G= | |
XM_011529968.1:c.1453-295G= | XP_011528270.1:n.1453-295G= | |
XM_011529969.1:c.1309-269G= | XP_011528271.1:n.1309-269G= | |
XM_011529970.1:c.1300-269G= | XP_011528272.1:n.1300-269G= |