Canonical Allele Identifier:
CA653585449
Community Standard Title: NC_000010.11:g.94762608T>G
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94762608T>G , CM000672.2:g.94762608T>G | GRCh38 |
| NC_000010.10:g.96522365T>G , CM000672.1:g.96522365T>G | GRCh37 |
| NC_000010.9:g.96512355T>G | NCBI36 |
| NG_008384.2:g.4903T>G | |
| NG_008384.3:g.4928T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| ENST00000464755.1:c.932-12450T>G | ENSP00000483243.1:n.932-12450T>G |