HGVS | Genome Assembly |
---|---|
NC_000014.9:g.77518022G= , CM000676.2:g.77518022G= | GRCh38 |
NC_000014.8:g.77984365G= , CM000676.1:g.77984365G= | GRCh37 |
NC_000014.7:g.77054118G= | NCBI36 |
NG_028282.1:g.103746C= , LRG_371:g.103746C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000686627.1:n.601+16C= | ||
ENST00000687688.1:n.1332+16C= | ||
ENST00000692906.1:n.1301+16C= | ||
ENST00000216484.7:c.1569+16C= MANE Select | ENSP00000216484.2:n.1569+16C= | |
ENST00000216484.6:c.1569+16C= | ENSP00000216484.2:n.1569+16C= | |
ENST00000556607.1:c.397+16C= | ENSP00000451029.1:n.397+16C= | |
NM_004863.3:c.1569+16C= , LRG_371t1:c.1569+16C= | NP_004854.1:n.1569+16C= | |
NM_004863.4:c.1569+16C= MANE Select | NP_004854.1:n.1569+16C= |