HGVS | Genome Assembly |
---|---|
NC_000013.11:g.46897104T>C , CM000675.2:g.46897104T>C | GRCh38 |
NC_000013.10:g.47471239T>C , CM000675.1:g.47471239T>C | GRCh37 |
NC_000013.9:g.46369240T>C | NCBI36 |
NG_013011.1:g.4931A>G |
HGVS | Amino-acid Change | |
---|---|---|
NM_001378924.1:c.-329+848A>G | NP_001365853.1:n.-329+848A>G |