HGVS | Genome Assembly |
---|---|
NC_000011.10:g.47339656T= , CM000673.2:g.47339656T= | GRCh38 |
NC_000011.9:g.47361207T= , CM000673.1:g.47361207T= | GRCh37 |
NC_000011.8:g.47317783T= | NCBI36 |
NG_007667.1:g.18047A= , LRG_386:g.18047A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000545968.6:c.2062A= MANE Select | ENSP00000442795.1:p.Thr688= | |
ENST00000256993.8:c.2062A= | ENSP00000256993.5:p.Thr688= | |
ENST00000399249.6:c.2062A= | ENSP00000382193.2:p.Thr688= | |
ENST00000544791.1:c.2062A= | ENSP00000444259.1:p.Thr688= | |
ENST00000545968.5:c.2062A= | ENSP00000442795.1:p.Thr688= | |
NM_000256.3:c.2062A= , LRG_386t1:c.2062A= MANE Select | NP_000247.2:p.Thr688= | |
XM_011520117.1:c.2044A= | XP_011518419.1:p.Thr682= | |
XM_011520118.1:c.2062A= | XP_011518420.1:p.Thr688= |