HGVS | Genome Assembly |
---|---|
NC_000001.11:g.165419874G>C , CM000663.2:g.165419874G>C | GRCh38 |
NC_000001.10:g.165389111G>C , CM000663.1:g.165389111G>C | GRCh37 |
NC_000001.9:g.163655735G>C | NCBI36 |
NG_029517.1:g.30482C>G | |
NG_029517.2:g.30482C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000359842.10:c.438C>G MANE Select | ENSP00000352900.5:p.Ser146= | |
ENST00000359842.9:c.438C>G | ENSP00000352900.5:p.Ser146= | |
ENST00000470566.1:n.363C>G | ||
ENST00000619224.1:c.69C>G | ENSP00000482458.1:p.Ser23= | |
NM_001256570.1:c.69C>G | NP_001243499.1:p.Ser23= | |
NM_001256571.1:c.69C>G | NP_001243500.1:p.Ser23= | |
NM_006917.4:c.438C>G | NP_008848.1:p.Ser146= | |
NM_006917.5:c.438C>G MANE Select | NP_008848.1:p.Ser146= | |
NM_001256571.2:c.69C>G | NP_001243500.1:p.Ser23= | |
NM_001256570.2:c.69C>G | NP_001243499.1:p.Ser23= |