HGVS | Genome Assembly |
---|---|
NC_000015.10:g.40471297C>T , CM000677.2:g.40471297C>T | GRCh38 |
NC_000015.9:g.40763496C>T , CM000677.1:g.40763496C>T | GRCh37 |
NC_000015.8:g.38550788C>T | NCBI36 |
NG_017074.1:g.5337C>T , LRG_600:g.5337C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000306243.7:c.84C>T MANE Select | ENSP00000307297.6:p.Gly28= | |
ENST00000306243.6:c.84C>T | ENSP00000307297.5:p.Gly28= | |
ENST00000559991.1:c.84C>T | ENSP00000453882.1:p.Gly28= | |
NM_130468.3:c.84C>T , LRG_600t1:c.84C>T | NP_569735.1:p.Gly28= | |
NM_130468.4:c.84C>T MANE Select | NP_569735.1:p.Gly28= |