HGVS | Genome Assembly |
---|---|
NC_000019.10:g.8377281C>T , CM000681.2:g.8377281C>T | GRCh38 |
NC_000019.9:g.8442165C>T , CM000681.1:g.8442165C>T | GRCh37 |
NC_000019.8:g.8348165C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000351593.9:c.-88+67725G>A (ELAVL1) | ENSP00000264073.6:n.-88+67725G>A | |
NR_038237.1:n.684-214G>A (RAB11B-AS1) |