HGVS | Genome Assembly |
---|---|
NC_000018.10:g.49878942T= , CM000680.2:g.49878942T= | GRCh38 |
NC_000018.9:g.47405312T= , CM000680.1:g.47405312T= | GRCh37 |
NC_000018.8:g.45659310T= | NCBI36 |
NG_012925.1:g.321140A= | |
NG_012925.2:g.321140A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000697218.1:n.33A= | ||
ENST00000697219.1:c.3073+3A= | ||
ENST00000285039.12:c.3276+3A= MANE Select | ENSP00000285039.6:n.3276+3A= | |
ENST00000285039.11:c.3276+3A= | ENSP00000285039.6:n.3276+3A= | |
ENST00000324581.10:c.705+3A= | ENSP00000315531.7:n.705+3A= | |
ENST00000589568.1:n.477+3A= | ||
ENST00000616031.4:c.1907-42209A= | ENSP00000479038.1:n.1907-42209A= | |
NM_001080467.2:c.3276+3A= | NP_001073936.1:n.3276+3A= | |
NM_001080467.3:c.3276+3A= MANE Select | NP_001073936.1:n.3276+3A= |