HGVS | Genome Assembly |
---|---|
NC_000017.11:g.39666016A= , CM000679.2:g.39666016A= | GRCh38 |
NC_000017.10:g.37822269A= , CM000679.1:g.37822269A= | GRCh37 |
NC_000017.9:g.35075795A= | NCBI36 |
NG_008892.1:g.5671A= , LRG_210:g.5671A= | |
NG_042278.1:g.3036A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000309889.3:c.411A= MANE Select | ENSP00000312624.2:p.Thr137= | |
ENST00000309889.2:c.411A= | ENSP00000312624.2:p.Thr137= | |
ENST00000578283.1:c.339A= | ENSP00000462787.1:p.Thr113= | |
NM_003673.3:c.411A= , LRG_210t1:c.411A= | NP_003664.1:p.Thr137= | |
NM_003673.4:c.411A= MANE Select | NP_003664.1:p.Thr137= |