HGVS | Genome Assembly |
---|---|
NC_000018.10:g.49878944C= , CM000680.2:g.49878944C= | GRCh38 |
NC_000018.9:g.47405314C= , CM000680.1:g.47405314C= | GRCh37 |
NC_000018.8:g.45659312C= | NCBI36 |
NG_012925.1:g.321138G= | |
NG_012925.2:g.321138G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000697218.1:n.31G= | ||
ENST00000697219.1:c.3073+1G= | ||
ENST00000285039.12:c.3276+1G= MANE Select | ENSP00000285039.6:n.3276+1G= | |
ENST00000285039.11:c.3276+1G= | ENSP00000285039.6:n.3276+1G= | |
ENST00000324581.10:c.705+1G= | ENSP00000315531.7:n.705+1G= | |
ENST00000589568.1:n.477+1G= | ||
ENST00000616031.4:c.1907-42211G= | ENSP00000479038.1:n.1907-42211G= | |
NM_001080467.2:c.3276+1G= | NP_001073936.1:n.3276+1G= | |
NM_001080467.3:c.3276+1G= MANE Select | NP_001073936.1:n.3276+1G= |