HGVS | Genome Assembly |
---|---|
NC_000005.10:g.173232668G= , CM000667.2:g.173232668G= | GRCh38 |
NC_000005.9:g.172659671G= , CM000667.1:g.172659671G= | GRCh37 |
NC_000005.8:g.172592277G= | NCBI36 |
NG_013340.1:g.7645C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000329198.5:c.876C= MANE Select | ENSP00000327758.4:p.Phe292= | |
ENST00000329198.4:c.876C= | ENSP00000327758.4:p.Phe292= | |
NM_001166175.1:c.*829C= | NP_001159647.1:n.*829C= | |
NM_001166176.1:c.*675C= | NP_001159648.1:n.*675C= | |
NM_004387.3:c.876C= | NP_004378.1:p.Phe292= | |
NM_004387.4:c.876C= MANE Select | NP_004378.1:p.Phe292= | |
NM_001166175.2:c.*829C= | NP_001159647.1:n.*829C= | |
NM_001166176.2:c.*675C= | NP_001159648.1:n.*675C= |