HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94051691A>T , CM000663.2:g.94051691A>T | GRCh38 |
NC_000001.10:g.94517247A>T , CM000663.1:g.94517247A>T | GRCh37 |
NC_000001.9:g.94289835A>T | NCBI36 |
NG_009073.1:g.74459T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.2595T>A MANE Select | ENSP00000359245.3:p.Tyr865Ter | |
ENST00000649773.1:c.2373T>A | ENSP00000496882.1:p.Tyr791Ter | |
ENST00000370225.3:c.2595T>A | ENSP00000359245.3:p.Tyr865Ter | |
ENST00000536513.5:c.-65+11483T>A | ENSP00000439707.2:n.-65+11483T>A | |
NM_000350.2:c.2595T>A | NP_000341.2:p.Tyr865Ter | |
NM_000350.3:c.2595T>A MANE Select | NP_000341.2:p.Tyr865Ter |