Canonical Allele Identifier:
CA2000589969
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112164712G= , CM000673.2:g.112164712G= | GRCh38 |
| NC_000011.9:g.112035435G= , CM000673.1:g.112035435G= | GRCh37 |
| NC_000011.8:g.111540645G= | NCBI36 |
| NG_028143.1:g.4406C= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000525987.5:n.320-5707G= | ||
| ENST00000531744.5:c.315-5707G= | ENSP00000456957.1:n.315-5707G= | |
| ENST00000532699.1:c.315-5707G= | ENSP00000456434.1:n.315-5707G= |