HGVS | Genome Assembly |
---|---|
NC_000006.12:g.43770182T>C , CM000668.2:g.43770182T>C | GRCh38 |
NC_000006.11:g.43737919T>C , CM000668.1:g.43737919T>C | GRCh37 |
NC_000006.10:g.43845897T>C | NCBI36 |
NG_008732.1:g.4967T>C |
HGVS | Amino-acid Change | |
---|---|---|
NM_001318876.2:c.945+240911T>C | NP_001305805.1:n.945+240911T>C |