HGVS | Genome Assembly |
---|---|
NC_000002.12:g.218813887T>A , CM000664.2:g.218813887T>A | GRCh38 |
NC_000002.11:g.219678610T>A , CM000664.1:g.219678610T>A | GRCh37 |
NC_000002.10:g.219386854T>A | NCBI36 |
NG_007959.1:g.37139T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258415.9:c.1018-134T>A MANE Select | ENSP00000258415.4:n.1018-134T>A | |
ENST00000258415.8:c.1018-134T>A | ENSP00000258415.4:n.1018-134T>A | |
ENST00000445971.1:c.*479-134T>A | ENSP00000404945.1:n.*479-134T>A | |
ENST00000466602.1:n.1140-134T>A | ||
ENST00000494263.5:n.1452-134T>A | ||
NM_000784.3:c.1018-134T>A | NP_000775.1:n.1018-134T>A | |
XM_017003488.2:c.598-134T>A | XP_016858977.1:n.598-134T>A | |
NM_000784.4:c.1018-134T>A MANE Select | NP_000775.1:n.1018-134T>A |