HGVS | Genome Assembly |
---|---|
NC_000019.10:g.8321446G>T , CM000681.2:g.8321446G>T | GRCh38 |
NC_000019.9:g.8386330G>T , CM000681.1:g.8386330G>T | GRCh37 |
NC_000019.8:g.8292330G>T | NCBI36 |
NG_028213.1:g.4951C>A | |
NG_028213.2:g.4951C>A | |
NG_050637.1:g.4947G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000351593.9:c.-87-59442C>A (ELAVL1) | ENSP00000264073.6:n.-87-59442C>A | |
ENST00000449223.3:n.289G>T (RPS28) |