Canonical Allele Identifier:
CA2469660368
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.2795902C= , CM000686.2:g.2795902C= | GRCh38 |
| NC_000024.9:g.2663943C= , CM000686.1:g.2663943C= | GRCh37 |
| NC_000024.8:g.2723943C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000679518.1:n.106+21163C= | ||
| ENST00000681787.1:n.106+21163C= | ||
| ENST00000681940.1:n.106+21163C= |