HGVS | Genome Assembly |
---|---|
NC_000011.10:g.47582056C= , CM000673.2:g.47582056C= | GRCh38 |
NC_000011.9:g.47603608C= , CM000673.1:g.47603608C= | GRCh37 |
NC_000011.8:g.47560184C= | NCBI36 |
NG_011946.1:g.8047C= | |
NG_011946.2:g.8047C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000263774.9:c.382-32C= MANE Select | ENSP00000263774.4:n.382-32C= | |
ENST00000531351.2:n.1410C= | ||
ENST00000677462.1:n.2824C= | ||
ENST00000678975.1:n.2607C= | ||
ENST00000263774.8:c.382-32C= | ENSP00000263774.4:n.382-32C= | |
ENST00000524568.1:n.485-32C= | ||
ENST00000525212.1:n.5C= | ||
ENST00000525378.5:n.288C= | ||
ENST00000533507.5:n.1276-32C= | ||
NM_004551.2:c.382-32C= | NP_004542.1:n.382-32C= | |
NM_004551.3:c.382-32C= MANE Select | NP_004542.1:n.382-32C= |