HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94780422T= , CM000672.2:g.94780422T= | GRCh38 |
NC_000010.10:g.96540179T= , CM000672.1:g.96540179T= | GRCh37 |
NC_000010.9:g.96530169T= | NCBI36 |
NG_008384.2:g.22717T= | |
NG_008384.3:g.22742T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371321.9:c.482-77T= MANE Select | ENSP00000360372.3:n.482-77T= | |
ENST00000645461.1:n.1535-77T= | ||
ENST00000371321.7:c.482-77T= | ENSP00000360372.3:n.482-77T= | |
ENST00000464755.1:c.1245-77T= | ENSP00000483243.1:n.1245-77T= | |
NM_000769.2:c.482-77T= | NP_000760.1:n.482-77T= | |
NM_000769.4:c.482-77T= MANE Select | NP_000760.1:n.482-77T= |