HGVS | Genome Assembly |
---|---|
NC_000008.11:g.102208098T= , CM000670.2:g.102208098T= | GRCh38 |
NC_000008.10:g.103220326T= , CM000670.1:g.103220326T= | GRCh37 |
NC_000008.9:g.103289502T= | NCBI36 |
NG_016617.1:g.36021A= , LRG_788:g.36021A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000251810.8:c.*35A= MANE Select | ENSP00000251810.3:n.*35A= | |
ENST00000251810.7:c.*35A= | ENSP00000251810.3:n.*35A= | |
ENST00000395910.6:n.478A= | ||
ENST00000522368.5:c.1260A= | ||
ENST00000621845.1:c.*35A= | ENSP00000484318.1:n.*35A= | |
NM_001172477.1:c.*35A= , LRG_788t1:c.*35A= | NP_001165948.1:n.*35A= | |
NM_001172478.1:c.*35A= | NP_001165949.1:n.*35A= | |
NM_015713.4:c.*35A= , LRG_788t2:c.*35A= | NP_056528.2:n.*35A= | |
NM_001172478.2:c.*35A= | NP_001165949.1:n.*35A= | |
NM_015713.5:c.*35A= MANE Select | NP_056528.2:n.*35A= |