HGVS | Genome Assembly |
---|---|
NC_000014.9:g.28768401C= , CM000676.2:g.28768401C= | GRCh38 |
NC_000014.8:g.29237607C= , CM000676.1:g.29237607C= | GRCh37 |
NC_000014.7:g.28307358C= | NCBI36 |
NG_009367.1:g.6321C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706482.1:c.1122C= | ENSP00000516406.1:p.Tyr374= | |
ENST00000313071.7:c.1122C= MANE Select | ENSP00000339004.3:p.Tyr374= | |
ENST00000313071.6:c.1122C= | ENSP00000339004.3:p.Tyr374= | |
NM_005249.4:c.1122C= | NP_005240.3:p.Tyr374= | |
NM_005249.5:c.1122C= MANE Select | NP_005240.3:p.Tyr374= |