HGVS | Genome Assembly |
---|---|
NC_000002.12:g.72891516C= , CM000664.2:g.72891516C= | GRCh38 |
NC_000002.11:g.73118645C= , CM000664.1:g.73118645C= | GRCh37 |
NC_000002.10:g.72972153C= | NCBI36 |
NG_008234.1:g.9134C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000234454.6:c.765C= MANE Select | ENSP00000234454.5:p.His255= | |
ENST00000234454.5:c.765C= | ENSP00000234454.5:p.His255= | |
ENST00000498749.1:n.710C= | ||
NM_003124.4:c.765C= | NP_003115.1:p.His255= | |
NM_003124.5:c.765C= MANE Select | NP_003115.1:p.His255= |