Canonical Allele Identifier:
CA12254308
Community Standard Title: NC_000006.12:g.155817575T>C
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.155817575T>C , CM000668.2:g.155817575T>C | GRCh38 |
| NC_000006.11:g.156138709T>C , CM000668.1:g.156138709T>C | GRCh37 |
| NC_000006.10:g.156180401T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_001744423.1:n.606-2905A>G | |
| XR_001744424.1:n.79+24156T>C | |
| XR_943142.1:n.79+24156T>C | |
| XR_943146.1:n.552-2905A>G |