HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99352874A>G , CM000666.2:g.99352874A>G | GRCh38 |
NC_000004.11:g.100274031A>G , CM000666.1:g.100274031A>G | GRCh37 |
NC_000004.10:g.100493054A>G | NCBI36 |
NG_011718.1:g.4887T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000515683.5:c.-199T>C | ENSP00000426083.1:n.-199T>C | |
NM_000669.4:c.-199T>C | NP_000660.1:n.-199T>C | |
NR_133005.1:n.172T>C | ||
XM_011531588.1:c.-199T>C | XP_011529890.1:n.-199T>C | |
XM_011531589.1:c.-439T>C | XP_011529891.1:n.-439T>C |