HGVS | Genome Assembly |
---|---|
NC_000002.12:g.27323104A>G , CM000664.2:g.27323104A>G | GRCh38 |
NC_000002.11:g.27545971A>G , CM000664.1:g.27545971A>G | GRCh37 |
NC_000002.10:g.27399475A>G | NCBI36 |
NG_008075.1:g.4461T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000357186.10:c.18+1329T>C | ENSP00000349713.6:n.18+1329T>C | |
XM_005264327.2:c.-182T>C | XP_005264384.1:n.-182T>C |