HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99352826T>C , CM000666.2:g.99352826T>C | GRCh38 |
NC_000004.11:g.100273983T>C , CM000666.1:g.100273983T>C | GRCh37 |
NC_000004.10:g.100493006T>C | NCBI36 |
NG_011718.1:g.4935A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000515683.5:c.-151A>G | ENSP00000426083.1:n.-151A>G | |
NM_000669.4:c.-151A>G | NP_000660.1:n.-151A>G | |
NR_133005.1:n.220A>G | ||
XM_011531588.1:c.-151A>G | XP_011529890.1:n.-151A>G | |
XM_011531589.1:c.-391A>G | XP_011529891.1:n.-391A>G |