Canonical Allele Identifier:
CA2773674429
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.155817632A>T , CM000668.2:g.155817632A>T | GRCh38 |
| NC_000006.11:g.156138766A>T , CM000668.1:g.156138766A>T | GRCh37 |
| NC_000006.10:g.156180458A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_943142.1:n.79+24213A>T | ||
| XR_943146.1:n.552-2962T>A | ||
| XR_001744423.1:n.606-2962T>A | ||
| XR_001744424.1:n.79+24213A>T |