Canonical Allele Identifier:
CA1093891267
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.121793305A>T , CM000668.2:g.121793305A>T | GRCh38 |
| NC_000006.11:g.122114451A>T , CM000668.1:g.122114451A>T | GRCh37 |
| NC_000006.10:g.122156150A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_942936.1:n.240+25690A>T | ||
| XR_942937.1:n.240+25690A>T | ||
| XR_942938.1:n.240+25690A>T | ||
| XR_942939.1:n.240+25690A>T | ||
| XR_942940.1:n.240+25690A>T | ||
| XR_942941.1:n.240+25690A>T | ||
| XR_942936.2:n.240+25690A>T | ||
| XR_942937.3:n.240+25690A>T |