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