HGVS | Genome Assembly |
---|---|
NC_000014.9:g.77518065T= , CM000676.2:g.77518065T= | GRCh38 |
NC_000014.8:g.77984408T= , CM000676.1:g.77984408T= | GRCh37 |
NC_000014.7:g.77054161T= | NCBI36 |
NG_028282.1:g.103703A= , LRG_371:g.103703A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000686627.1:n.574A= | ||
ENST00000687688.1:n.1305A= | ||
ENST00000692906.1:n.1274A= | ||
ENST00000216484.7:c.1542A= MANE Select | ENSP00000216484.2:p.Ala514= | |
ENST00000216484.6:c.1542A= | ENSP00000216484.2:p.Ala514= | |
ENST00000556607.1:c.370A= | ENSP00000451029.1:n.370A= | |
NM_004863.3:c.1542A= , LRG_371t1:c.1542A= | NP_004854.1:p.Ala514= | |
NM_004863.4:c.1542A= MANE Select | NP_004854.1:p.Ala514= |