HGVS | Genome Assembly |
---|---|
NC_000003.12:g.143531306C= , CM000665.2:g.143531306C= | GRCh38 |
NC_000003.11:g.143250148C= , CM000665.1:g.143250148C= | GRCh37 |
NC_000003.10:g.144732838C= | NCBI36 |
NG_017077.1:g.322226G= | |
NG_017077.2:g.322226G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000316549.11:c.1089+21056G= MANE Select | ENSP00000320246.6:n.1089+21056G= | |
ENST00000316549.10:c.1089+21056G= | ENSP00000320246.6:n.1089+21056G= | |
NM_173653.3:c.1089+21056G= | NP_775924.1:n.1089+21056G= | |
XM_011512703.1:c.441+21056G= | XP_011511005.1:n.441+21056G= | |
XM_011512703.3:c.441+21056G= | XP_011511005.1:n.441+21056G= | |
XM_017006202.2:c.1089+21056G= | XP_016861691.1:n.1089+21056G= | |
XM_017006203.1:c.738+21056G= | XP_016861692.1:n.738+21056G= | |
NM_173653.4:c.1089+21056G= MANE Select | NP_775924.1:n.1089+21056G= |