HGVS | Genome Assembly |
---|---|
NC_000022.11:g.50697525T>A , CM000684.2:g.50697525T>A | GRCh38 |
NC_000022.10:g.51135953T>A , CM000684.1:g.51135953T>A | GRCh37 |
NC_000022.9:g.49482819T>A | NCBI36 |
NG_008607.2:g.27884T>A | |
NG_070230.1:g.33103T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262795.7:c.948-39T>A | ENSP00000489147.2:n.948-39T>A | |
ENST00000414786.7:n.1532-39T>A | ||
ENST00000673971.2:c.1305-39T>A | ENSP00000501192.1:n.1305-39T>A | |
ENST00000262795.6:c.948-39T>A | ENSP00000489147.2:n.948-39T>A | |
ENST00000673971.1:c.1305-39T>A | ENSP00000501192.1:n.1305-39T>A | |
ENST00000262795.5:c.1345-40T>A | ENSP00000489147.1:n.1345-40T>A | |
ENST00000414786.6:n.1532-39T>A | ||
ENST00000445220.5:c.1326-39T>A | ENSP00000489407.1:n.1326-39T>A |