Canonical Allele Identifier:
CA952073742
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.114430333A>T , CM000674.2:g.114430333A>T | GRCh38 |
| NC_000012.11:g.114868138A>T , CM000674.1:g.114868138A>T | GRCh37 |
| NC_000012.10:g.113352521A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_945376.1:n.151-5256T>A | ||
| XR_001749319.1:n.177-5256T>A | ||
| XR_945376.2:n.177-5256T>A |