HGVS | Genome Assembly |
---|---|
NC_000022.11:g.45293369G= , CM000684.2:g.45293369G= | GRCh38 |
NC_000022.10:g.45689250G= , CM000684.1:g.45689250G= | GRCh37 |
NC_000022.9:g.44067914G= | NCBI36 |
NG_016203.1:g.13383G= | |
NG_016203.2:g.13383G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000216211.9:c.704+56G= MANE Select | ENSP00000216211.4:n.704+56G= | |
ENST00000216211.8:c.704+56G= | ENSP00000216211.4:n.704+56G= | |
ENST00000396082.2:c.341+56G= | ENSP00000379391.2:n.341+56G= | |
NM_001167574.1:c.341+56G= | NP_001161046.1:n.341+56G= | |
NM_006953.3:c.704+56G= | NP_008884.1:n.704+56G= | |
XM_011530364.1:c.710+56G= | XP_011528666.1:n.710+56G= | |
XM_011530365.1:c.347+56G= | XP_011528667.1:n.347+56G= | |
NM_006953.4:c.704+56G= MANE Select | NP_008884.1:n.704+56G= | |
NM_001167574.2:c.341+56G= | NP_001161046.1:n.341+56G= |