HGVS | Genome Assembly |
---|---|
NC_000022.11:g.45293132T= , CM000684.2:g.45293132T= | GRCh38 |
NC_000022.10:g.45689013T= , CM000684.1:g.45689013T= | GRCh37 |
NC_000022.9:g.44067677T= | NCBI36 |
NG_016203.1:g.13146T= | |
NG_016203.2:g.13146T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000216211.9:c.572-49T= MANE Select | ENSP00000216211.4:n.572-49T= | |
ENST00000216211.8:c.572-49T= | ENSP00000216211.4:n.572-49T= | |
ENST00000396082.2:c.209-49T= | ENSP00000379391.2:n.209-49T= | |
NM_001167574.1:c.209-49T= | NP_001161046.1:n.209-49T= | |
NM_006953.3:c.572-49T= | NP_008884.1:n.572-49T= | |
XM_011530364.1:c.578-49T= | XP_011528666.1:n.578-49T= | |
XM_011530365.1:c.215-49T= | XP_011528667.1:n.215-49T= | |
NM_006953.4:c.572-49T= MANE Select | NP_008884.1:n.572-49T= | |
NM_001167574.2:c.209-49T= | NP_001161046.1:n.209-49T= |