HGVS | Genome Assembly |
---|---|
NC_000015.10:g.50140321A>C , CM000677.2:g.50140321A>C | GRCh38 |
NC_000015.9:g.50432518A>C , CM000677.1:g.50432518A>C | GRCh37 |
NC_000015.8:g.48219810A>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000558829.1:c.-42-33313T>G | ENSP00000453539.1:n.-42-33313T>G | |
XM_011522056.1:c.-42-33313T>G | XP_011520358.1:n.-42-33313T>G | |
XM_011522056.3:c.-42-33313T>G | XP_011520358.3:n.-42-33313T>G | |
XM_017022587.2:c.-42-33313T>G | XP_016878076.2:n.-42-33313T>G |