Canonical Allele Identifier:
CA1877121788
Community Standard Title: NC_000009.12:g.121565769T=
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.121565769T= , CM000671.2:g.121565769T= | GRCh38 |
| NC_000009.11:g.124328048T= , CM000671.1:g.124328048T= | GRCh37 |
| NC_000009.10:g.123367869T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_001746560.1:n.2055+1082A= |