HGVS | Genome Assembly |
---|---|
NC_000014.9:g.36663376T>A , CM000676.2:g.36663376T>A | GRCh38 |
NC_000014.8:g.37132581T>A , CM000676.1:g.37132581T>A | GRCh37 |
NC_000014.7:g.36202332T>A | NCBI36 |
NG_013357.1:g.10809T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361487.7:c.484T>A MANE Select | ENSP00000355245.6:p.Tyr162Asn | |
ENST00000361487.6:c.484T>A | ENSP00000355245.6:p.Tyr162Asn | |
ENST00000402703.6:c.484T>A | ENSP00000384817.2:p.Tyr162Asn | |
ENST00000554201.1:c.-78T>A | ENSP00000450434.1:n.-78T>A | |
NM_006194.3:c.484T>A | NP_006185.1:p.Tyr162Asn | |
NM_001372076.1:c.484T>A MANE Select | NP_001359005.1:p.Tyr162Asn | |
NM_006194.4:c.484T>A | NP_006185.1:p.Tyr162Asn |