HGVS | Genome Assembly |
---|---|
NC_000019.10:g.8321444C>A , CM000681.2:g.8321444C>A | GRCh38 |
NC_000019.9:g.8386328C>A , CM000681.1:g.8386328C>A | GRCh37 |
NC_000019.8:g.8292328C>A | NCBI36 |
NG_028213.1:g.4953G>T | |
NG_028213.2:g.4953G>T | |
NG_050637.1:g.4945C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000351593.9:c.-87-59440G>T (ELAVL1) | ENSP00000264073.6:n.-87-59440G>T | |
ENST00000449223.3:n.287C>A (RPS28) |