Canonical Allele Identifier:
CA1247519092
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.41534625G= , CM000664.2:g.41534625G= | GRCh38 |
| NC_000002.11:g.41761765G= , CM000664.1:g.41761765G= | GRCh37 |
| NC_000002.10:g.41615269G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_939996.1:n.181+3101C= | ||
| XR_939997.1:n.146+3101C= | ||
| XR_939997.2:n.9529+3101C= |