HGVS | Genome Assembly |
---|---|
NC_000001.11:g.179575981T>C , CM000663.2:g.179575981T>C | GRCh38 |
NC_000001.10:g.179545116T>C , CM000663.1:g.179545116T>C | GRCh37 |
NC_000001.9:g.177811739T>C | NCBI36 |
NG_007535.1:g.4969A>G , LRG_887:g.4969A>G |
HGVS | Amino-acid Change | |
---|---|---|
XM_017002298.1:c.-117A>G | XP_016857787.1:n.-117A>G | |
XM_017002299.1:c.-117A>G | XP_016857788.1:n.-117A>G |