Canonical Allele Identifier:
CA2838713251
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.29376298T>C , CM000679.2:g.29376298T>C | GRCh38 |
| NC_000017.10:g.27703316T>C , CM000679.1:g.27703316T>C | GRCh37 |
| NC_000017.9:g.24727442T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011525588.1:c.1008-5993A>G | XP_011523890.1:n.1008-5993A>G |