HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21176732T= , CM000674.2:g.21176732T= | GRCh38 |
NC_000012.11:g.21329666T= , CM000674.1:g.21329666T= | GRCh37 |
NC_000012.10:g.21220933T= | NCBI36 |
NG_011745.1:g.50539T= , LRG_1022:g.50539T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256958.3:c.360-44T= MANE Select | ENSP00000256958.2:n.360-44T= | |
ENST00000256958.2:c.360-44T= | ENSP00000256958.2:n.360-44T= | |
ENST00000543498.5:c.426-44T= | ||
NM_006446.4:c.360-44T= , LRG_1022t1:c.360-44T= | NP_006437.3:n.360-44T= | |
NM_006446.5:c.360-44T= MANE Select | NP_006437.3:n.360-44T= |