Canonical Allele Identifier:
CA1697889703
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.30897492C= , CM000669.2:g.30897492C= | GRCh38 |
| NC_000007.13:g.30937107C= , CM000669.1:g.30937107C= | GRCh37 |
| NC_000007.12:g.30903632C= | NCBI36 |
| NG_007475.2:g.49099C= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000509504.2:c.621+14499C= |