HGVS | Genome Assembly |
---|---|
NC_000011.10:g.47342707A>T , CM000673.2:g.47342707A>T | GRCh38 |
NC_000011.9:g.47364258A>T , CM000673.1:g.47364258A>T | GRCh37 |
NC_000011.8:g.47320834A>T | NCBI36 |
NG_007667.1:g.14996T>A , LRG_386:g.14996T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000545968.6:c.1495T>A MANE Select | ENSP00000442795.1:p.Phe499Ile | |
ENST00000256993.8:c.1495T>A | ENSP00000256993.5:p.Phe499Ile | |
ENST00000399249.6:c.1495T>A | ENSP00000382193.2:p.Phe499Ile | |
ENST00000544791.1:c.1495T>A | ENSP00000444259.1:p.Phe499Ile | |
ENST00000545968.5:c.1495T>A | ENSP00000442795.1:p.Phe499Ile | |
NM_000256.3:c.1495T>A , LRG_386t1:c.1495T>A MANE Select | NP_000247.2:p.Phe499Ile | |
XM_011520117.1:c.1477T>A | XP_011518419.1:p.Phe493Ile | |
XM_011520118.1:c.1495T>A | XP_011518420.1:p.Phe499Ile |