HGVS | Genome Assembly |
---|---|
NC_000024.10:g.6909840A>C , CM000686.2:g.6909840A>C | GRCh38 |
NC_000024.9:g.6777881A>C , CM000686.1:g.6777881A>C | GRCh37 |
NC_000024.8:g.6837881A>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000651267.2:c.-113+1833T>G (AMELY) MANE Select | ENSP00000498344.1:n.-113+1833T>G | |
ENST00000651267.1:c.-113+1833T>G (AMELY) | ENSP00000498344.1:n.-113+1833T>G | |
XM_011531472.1:c.-113+1833T>G (AMELY) | XP_011529774.1:n.-113+1833T>G | |
XM_024452497.1:c.-614A>C (TBL1Y) | XP_024308265.1:n.-614A>C | |
NM_001143.2:c.-113+1833T>G (AMELY) MANE Select | NP_001134.1:n.-113+1833T>G |