HGVS | Genome Assembly |
---|---|
NC_000007.14:g.37801932A>T , CM000669.2:g.37801932A>T | GRCh38 |
NC_000007.13:g.37841534A>T , CM000669.1:g.37841534A>T | GRCh37 |
NC_000007.12:g.37808059A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000461610.5:n.233-27323A>T (GPR141) | ||
ENST00000476620.1:c.-109-55342A>T (EPDR1) | ENSP00000425858.1:n.-109-55342A>T |