Canonical Allele Identifier:
CA1618478398
Community Standard Title: NC_000006.12:g.29850791T=
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.29850791T= , CM000668.2:g.29850791T= | GRCh38 |
| NC_000006.11:g.29818568T= , CM000668.1:g.29818568T= | GRCh37 |
| NC_000006.10:g.29926547T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| ENST00000647952.1:n.2321-162A= | |
| XR_926680.1:n.207-162A= | |
| XR_926680.2:n.207-162A= | |
| XR_926681.1:n.207-162A= | |
| XR_926681.2:n.207-162A= | |
| XR_926682.1:n.206+1531A= | |
| XR_926682.2:n.206+1531A= |