HGVS | Genome Assembly |
---|---|
NC_000020.11:g.38363182T= , CM000682.2:g.38363182T= | GRCh38 |
NC_000020.10:g.36991836T= , CM000682.1:g.36991836T= | GRCh37 |
NC_000020.9:g.36425250T= | NCBI36 |
NG_034239.1:g.21772T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000217407.3:c.653-793T= MANE Select | ENSP00000217407.2:n.653-793T= | |
ENST00000217407.2:c.653-793T= | ENSP00000217407.2:n.653-793T= | |
NM_004139.4:c.653-793T= | NP_004130.2:n.653-793T= | |
NM_004139.5:c.653-793T= MANE Select | NP_004130.2:n.653-793T= |