Canonical Allele Identifier:
CA1839005951
Community Standard Title: NC_000009.12:g.21701433T=
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.21701433T= , CM000671.2:g.21701433T= | GRCh38 |
| NC_000009.11:g.21701432T= , CM000671.1:g.21701432T= | GRCh37 |
| NC_000009.10:g.21691432T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_001746563.2:n.384+1484A= |