HGVS | Genome Assembly |
---|---|
NC_000017.11:g.45727828T>G , CM000679.2:g.45727828T>G | GRCh38 |
NC_000017.10:g.43805194T>G , CM000679.1:g.43805194T>G | GRCh37 |
NC_000017.9:g.41160977T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000587305.1:n.447+54926T>G | ||
ENST00000634540.1:c.-492-79182T>G | ENSP00000488912.1:n.-492-79182T>G | |
NM_001256299.2:c.-492-79182T>G | NP_001243228.1:n.-492-79182T>G | |
NM_001303016.1:c.-185+54926T>G | NP_001289945.1:n.-185+54926T>G | |
NM_001256299.3:c.-492-79182T>G | NP_001243228.1:n.-492-79182T>G |