HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99352918A>G , CM000666.2:g.99352918A>G | GRCh38 |
NC_000004.11:g.100274075A>G , CM000666.1:g.100274075A>G | GRCh37 |
NC_000004.10:g.100493098A>G | NCBI36 |
NG_011718.1:g.4843T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000515683.5:c.-243T>C | ENSP00000426083.1:n.-243T>C | |
NM_000669.4:c.-243T>C | NP_000660.1:n.-243T>C | |
NR_133005.1:n.128T>C | ||
XM_011531588.1:c.-243T>C | XP_011529890.1:n.-243T>C | |
XM_011531589.1:c.-483T>C | XP_011529891.1:n.-483T>C |