HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99352863A>C , CM000666.2:g.99352863A>C | GRCh38 |
NC_000004.11:g.100274020A>C , CM000666.1:g.100274020A>C | GRCh37 |
NC_000004.10:g.100493043A>C | NCBI36 |
NG_011718.1:g.4898T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000515683.5:c.-188T>G | ENSP00000426083.1:n.-188T>G | |
NM_000669.4:c.-188T>G | NP_000660.1:n.-188T>G | |
NR_133005.1:n.183T>G | ||
XM_011531588.1:c.-188T>G | XP_011529890.1:n.-188T>G | |
XM_011531589.1:c.-428T>G | XP_011529891.1:n.-428T>G |