HGVS | Genome Assembly |
---|---|
NC_000022.11:g.42126100C>T , CM000684.2:g.42126100C>T | GRCh38 |
NC_000022.10:g.42522105C>T , CM000684.1:g.42522105C>T | GRCh37 |
NC_000022.9:g.40852049C>T | NCBI36 |
NG_008376.3:g.8892G>A | |
NG_008376.4:g.9711G>A |
HGVS | Amino-acid Change | |
---|---|---|
XM_011529966.1:c.1453-147G>A | XP_011528268.1:n.1453-147G>A | |
XM_011529967.1:c.1453-147G>A | XP_011528269.1:n.1453-147G>A | |
XM_011529968.1:c.1453-173G>A | XP_011528270.1:n.1453-173G>A | |
XM_011529969.1:c.1309-147G>A | XP_011528271.1:n.1309-147G>A | |
XM_011529970.1:c.1300-147G>A | XP_011528272.1:n.1300-147G>A |