HGVS | Genome Assembly |
---|---|
NC_000022.11:g.18078368G= , CM000684.2:g.18078368G= | GRCh38 |
NC_000022.10:g.18561134G= , CM000684.1:g.18561134G= | GRCh37 |
NC_000022.9:g.16941134G= | NCBI36 |
NG_008339.1:g.5449G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000399744.8:c.-9G= MANE Select | ENSP00000382648.4:n.-9G= | |
ENST00000474897.6:c.-9G= | ENSP00000434235.2:n.-9G= | |
ENST00000329627.11:c.-9G= | ENSP00000331106.5:n.-9G= | |
ENST00000399744.7:c.-9G= | ENSP00000382648.3:n.-9G= | |
ENST00000474897.5:c.-9G= | ENSP00000434235.1:n.-9G= | |
ENST00000610387.4:c.-9G= | ENSP00000482091.1:n.-9G= | |
NM_001127649.2:c.-9G= | NP_001121121.1:n.-9G= | |
NM_001199319.1:c.-9G= | NP_001186248.1:n.-9G= | |
NM_017929.5:c.-9G= | NP_060399.1:n.-9G= | |
NM_001127649.3:c.-9G= MANE Select | NP_001121121.1:n.-9G= | |
NM_001199319.2:c.-9G= | NP_001186248.1:n.-9G= | |
NM_017929.6:c.-9G= | NP_060399.1:n.-9G= |