Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.8321450T>C , CM000681.2:g.8321450T>C | GRCh38 |
| NC_000019.9:g.8386334T>C , CM000681.1:g.8386334T>C | GRCh37 |
| NC_000019.8:g.8292334T>C | NCBI36 |
| NG_028213.1:g.4947A>G | |
| NG_028213.2:g.4947A>G | |
| NG_050637.1:g.4951T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000351593.9:c.-87-59446A>G (ELAVL1) | ENSP00000264073.6:n.-87-59446A>G | |
| ENST00000449223.3:n.293T>C (RPS28) |