Canonical Allele Identifier:
CA2612218603
Gene:
Linked Data
gnomAD v4:
11-6318892-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6318892T>C , CM000673.2:g.6318892T>C | GRCh38 |
| NC_000011.9:g.6340122T>C , CM000673.1:g.6340122T>C | GRCh37 |
| NC_000011.8:g.6296698T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_930997.1:n.720+672T>C |