HGVS | Genome Assembly |
---|---|
NC_000022.11:g.50697466G>T , CM000684.2:g.50697466G>T | GRCh38 |
NC_000022.10:g.51135894G>T , CM000684.1:g.51135894G>T | GRCh37 |
NC_000022.9:g.49482760G>T | NCBI36 |
NG_008607.2:g.27825G>T | |
NG_070230.1:g.33044G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262795.7:c.948-98G>T | ENSP00000489147.2:n.948-98G>T | |
ENST00000414786.7:n.1532-98G>T | ||
ENST00000673971.2:c.1305-98G>T | ENSP00000501192.1:n.1305-98G>T | |
ENST00000262795.6:c.948-98G>T | ENSP00000489147.2:n.948-98G>T | |
ENST00000673971.1:c.1305-98G>T | ENSP00000501192.1:n.1305-98G>T | |
ENST00000262795.5:c.1345-99G>T | ENSP00000489147.1:n.1345-99G>T | |
ENST00000414786.6:n.1532-98G>T | ||
ENST00000445220.5:c.1326-98G>T | ENSP00000489407.1:n.1326-98G>T |