HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99352882C= , CM000666.2:g.99352882C= | GRCh38 |
NC_000004.11:g.100274039C= , CM000666.1:g.100274039C= | GRCh37 |
NC_000004.10:g.100493062C= | NCBI36 |
NG_011718.1:g.4879G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000515683.5:c.-207G= | ENSP00000426083.1:n.-207G= | |
NM_000669.4:c.-207G= | NP_000660.1:n.-207G= | |
NR_133005.1:n.164G= | ||
XM_011531588.1:c.-207G= | XP_011529890.1:n.-207G= | |
XM_011531589.1:c.-447G= | XP_011529891.1:n.-447G= |