HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99352856C>T , CM000666.2:g.99352856C>T | GRCh38 |
NC_000004.11:g.100274013C>T , CM000666.1:g.100274013C>T | GRCh37 |
NC_000004.10:g.100493036C>T | NCBI36 |
NG_011718.1:g.4905G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000515683.5:c.-181G>A | ENSP00000426083.1:n.-181G>A | |
NM_000669.4:c.-181G>A | NP_000660.1:n.-181G>A | |
NR_133005.1:n.190G>A | ||
XM_011531588.1:c.-181G>A | XP_011529890.1:n.-181G>A | |
XM_011531589.1:c.-421G>A | XP_011529891.1:n.-421G>A |