HGVS | Genome Assembly |
---|---|
NC_000012.12:g.91111699A>G , CM000674.2:g.91111699A>G | GRCh38 |
NC_000012.11:g.91505476A>G , CM000674.1:g.91505476A>G | GRCh37 |
NC_000012.10:g.90029607A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266718.4:c.-323T>C | ENSP00000266718.4:n.-323T>C | |
NM_002345.3:c.-323T>C | NP_002336.1:n.-323T>C |