HGVS | Genome Assembly |
---|---|
NC_000023.11:g.47573099C= , CM000685.2:g.47573099C= | GRCh38 |
NC_000023.10:g.47432498C= , CM000685.1:g.47432498C= | GRCh37 |
NC_000023.9:g.47317442C= | NCBI36 |
NG_008437.1:g.51759G= | |
NG_016339.1:g.16983C= | |
NG_016339.2:g.16983C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295987.13:c.1983-100G= MANE Select | ENSP00000295987.7:n.1983-100G= | |
ENST00000340666.5:c.1983-138G= | ENSP00000343206.4:n.1983-138G= | |
ENST00000640721.1:c.71-138G= | ENSP00000492857.1:n.71-138G= | |
ENST00000295987.11:c.1983-100G= | ENSP00000295987.7:n.1983-100G= | |
ENST00000340666.4:c.1983-138G= | ENSP00000343206.4:n.1983-138G= | |
NM_006950.3:c.1983-100G= MANE Select | NP_008881.2:n.1983-100G= | |
NM_133499.2:c.1983-138G= | NP_598006.1:n.1983-138G= |