HGVS | Genome Assembly |
---|---|
NC_000001.11:g.28843047T>C , CM000663.2:g.28843047T>C | GRCh38 |
NC_000001.10:g.29169559T>C , CM000663.1:g.29169559T>C | GRCh37 |
NC_000001.9:g.29042146T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000234961.7:c.228-15907T>C MANE Select | ENSP00000234961.2:n.228-15907T>C | |
ENST00000234961.6:c.228-15907T>C | ENSP00000234961.2:n.228-15907T>C | |
ENST00000621425.1:c.228-15907T>C | ENSP00000477970.1:n.228-15907T>C | |
NM_000911.3:c.228-15907T>C | NP_000902.3:n.228-15907T>C | |
NM_000911.4:c.228-15907T>C MANE Select | NP_000902.3:n.228-15907T>C |