HGVS | Genome Assembly |
---|---|
NC_000012.12:g.91111605A>G , CM000674.2:g.91111605A>G | GRCh38 |
NC_000012.11:g.91505382A>G , CM000674.1:g.91505382A>G | GRCh37 |
NC_000012.10:g.90029513A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266718.4:c.-229T>C | ENSP00000266718.4:n.-229T>C | |
NM_002345.3:c.-229T>C | NP_002336.1:n.-229T>C |