HGVS | Genome Assembly |
---|---|
NC_000008.11:g.102208123G= , CM000670.2:g.102208123G= | GRCh38 |
NG_016617.1:g.35996C= , LRG_788:g.35996C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000251810.8:c.*10C= MANE Select | ENSP00000251810.3:n.*10C= | |
ENST00000251810.7:c.*10C= | ENSP00000251810.3:n.*10C= | |
ENST00000395910.6:n.453C= | ||
ENST00000522368.5:c.1235C= | ||
ENST00000621845.1:c.*10C= | ENSP00000484318.1:n.*10C= | |
NM_001172477.1:c.*10C= , LRG_788t1:c.*10C= | NP_001165948.1:n.*10C= | |
NM_001172478.1:c.*10C= | NP_001165949.1:n.*10C= | |
NM_015713.4:c.*10C= , LRG_788t2:c.*10C= | NP_056528.2:n.*10C= | |
NM_001172478.2:c.*10C= | NP_001165949.1:n.*10C= | |
NM_015713.5:c.*10C= MANE Select | NP_056528.2:n.*10C= |