Canonical Allele Identifier:
CA1662343685
Gene:
Linked Data
dbSNP Id:
rs17299841
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.127700658A>G , CM000668.2:g.127700658A>G | GRCh38 |
| NC_000006.11:g.128021803A>G , CM000668.1:g.128021803A>G | GRCh37 |
| NC_000006.10:g.128063496A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_002956393.1:n.2017T>C | ||
| XR_002956394.1:n.2017T>C |