HGVS | Genome Assembly |
---|---|
NC_000017.11:g.21380962G= , CM000679.2:g.21380962G= | GRCh38 |
NC_000017.10:g.21284274G= , CM000679.1:g.21284274G= | GRCh37 |
NC_000017.9:g.21224867G= | NCBI36 |
NG_042809.1:g.9576G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000583088.6:c.-179+4049G= MANE Select | ENSP00000463778.1:n.-179+4049G= | |
ENST00000583088.5:c.-179+4049G= | ENSP00000463778.1:n.-179+4049G= | |
NM_021012.4:c.-179+4049G= | NP_066292.2:n.-179+4049G= | |
XM_005256625.3:c.-179+3636G= | XP_005256682.1:n.-179+3636G= | |
XM_005256625.5:c.-179+3636G= | XP_005256682.1:n.-179+3636G= | |
NM_021012.5:c.-179+4049G= MANE Select | NP_066292.2:n.-179+4049G= |