HGVS | Genome Assembly |
---|---|
NC_000007.14:g.79453745G>T , CM000669.2:g.79453745G>T | GRCh38 |
NC_000007.13:g.79083061G>T , CM000669.1:g.79083061G>T | GRCh37 |
NC_000007.12:g.78920997G>T | NCBI36 |
NG_011487.1:g.4830C>A | |
NG_011487.2:g.4830C>A |
HGVS | Amino-acid Change | |
---|---|---|
NR_038345.1:n.235+554G>T (MAGI2-AS3) | ||
NR_038346.1:n.304+90G>T (MAGI2-AS3) | ||
XM_011516718.1:c.-425C>A (MAGI2) | XP_011515020.1:n.-425C>A | |
XM_011516723.1:c.-425C>A (MAGI2) | XP_011515025.1:n.-425C>A | |
XM_011516724.1:c.-425C>A (MAGI2) | XP_011515026.1:n.-425C>A | |
XM_011516725.1:c.-425C>A (MAGI2) | XP_011515027.1:n.-425C>A |