HGVS | Genome Assembly |
---|---|
NC_000005.10:g.10286363A>C , CM000667.2:g.10286363A>C | GRCh38 |
NC_000005.9:g.10286475A>C , CM000667.1:g.10286475A>C | GRCh37 |
NC_000005.8:g.10339475A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000296658.4:c.457T>G MANE Select | ENSP00000296658.3:p.Ser153Ala | |
ENST00000296658.3:c.457T>G | ENSP00000296658.3:p.Ser153Ala | |
ENST00000506821.1:n.711T>G | ||
ENST00000510532.5:n.525T>G | ||
ENST00000511963.5:n.565T>G | ||
NM_138809.3:c.457T>G | NP_620164.1:p.Ser153Ala | |
NM_138809.4:c.457T>G MANE Select | NP_620164.1:p.Ser153Ala |