HGVS | Genome Assembly |
---|---|
NC_000007.14:g.74789365T>G , CM000669.2:g.74789365T>G | GRCh38 |
NC_000007.13:g.74203709T>G , CM000669.1:g.74203709T>G | GRCh37 |
NC_000007.12:g.73841645T>G | NCBI36 |
NG_009078.2:g.20402T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000289473.10:c.*205T>G | ENSP00000289473.4:n.*205T>G | |
NM_000265.5:c.*205T>G | NP_000256.4:n.*205T>G | |
XM_005250543.3:c.*299T>G | XP_005250600.2:n.*299T>G | |
XM_011516498.1:c.*252T>G | XP_011514800.1:n.*252T>G | |
XM_011516501.1:c.*205T>G | XP_011514803.1:n.*205T>G | |
NM_000265.6:c.*205T>G | NP_000256.4:n.*205T>G |