HGVS | Genome Assembly |
---|---|
NC_000002.12:g.79405188T>C , CM000664.2:g.79405188T>C | GRCh38 |
NC_000002.11:g.79632314T>C , CM000664.1:g.79632314T>C | GRCh37 |
NC_000002.10:g.79485822T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000466387.5:c.-135+31175T>C | ENSP00000418191.1:n.-135+31175T>C | |
NM_001399737.1:c.-135+31175T>C | NP_001386666.1:n.-135+31175T>C |