HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42536786G= , CM000679.2:g.42536786G= | GRCh38 |
NC_000017.10:g.40688804G= , CM000679.1:g.40688804G= | GRCh37 |
NC_000017.9:g.37942330G= | NCBI36 |
NG_011552.1:g.5854G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000225927.7:c.383+131G= MANE Select | ENSP00000225927.1:n.383+131G= | |
ENST00000225927.6:c.383+131G= | ENSP00000225927.1:n.383+131G= | |
ENST00000586516.5:c.133+131G= | ||
ENST00000591587.1:c.126+131G= | ENSP00000467836.1:n.126+131G= | |
NM_000263.3:c.383+131G= | NP_000254.2:n.383+131G= | |
XM_006721920.2:c.-360+131G= | XP_006721983.1:n.-360+131G= | |
XM_011524840.1:c.-360+131G= | XP_011523142.1:n.-360+131G= | |
XM_024450771.1:c.384-31G= | XP_024306539.1:n.384-31G= | |
NM_000263.4:c.383+131G= MANE Select | NP_000254.2:n.383+131G= |