HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41586533C= , CM000679.2:g.41586533C= | GRCh38 |
NC_000017.10:g.39742785C= , CM000679.1:g.39742785C= | GRCh37 |
NC_000017.9:g.36996311C= | NCBI36 |
NG_008624.1:g.5363G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.302G= MANE Select | ENSP00000167586.6:p.Gly101= | |
ENST00000167586.6:c.302G= | ENSP00000167586.6:p.Gly101= | |
NM_000526.4:c.302G= | NP_000517.2:p.Gly101= | |
NM_000526.5:c.302G= MANE Select | NP_000517.3:p.Gly101= |