Canonical Allele Identifier:
CA2332763282
Gene:
Linked Data
dbSNP Id:
rs1971154739
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.33521972A>C , CM000681.2:g.33521972A>C | GRCh38 |
| NC_000019.9:g.34012878A>C , CM000681.1:g.34012878A>C | GRCh37 |
| NC_000019.8:g.38704718A>C | NCBI36 |
| NG_013358.1:g.4922T>G | |
| NG_013358.2:g.4922T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_935918.1:n.31A>C | ||
| XR_935919.1:n.26A>C | ||
| XR_001754035.2:n.39A>C | ||
| XR_935918.2:n.39A>C |