Canonical Allele Identifier:
CA1846956621
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.37579556G= , CM000671.2:g.37579556G= | GRCh38 |
| NC_000009.11:g.37579553G= , CM000671.1:g.37579553G= | GRCh37 |
| NC_000009.10:g.37569553G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000537239.2:c.282+9255C= | ENSP00000457849.1:n.282+9255C= | |
| ENST00000541804.1:n.62+9257C= | ||
| ENST00000544475.5:n.122+9197C= |