Canonical Allele Identifier:
CA2332763334
Gene:
Linked Data
dbSNP Id:
rs1971156393
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.33522044G>T , CM000681.2:g.33522044G>T | GRCh38 |
| NC_000019.9:g.34012950G>T , CM000681.1:g.34012950G>T | GRCh37 |
| NC_000019.8:g.38704790G>T | NCBI36 |
| NG_013358.1:g.4850C>A | |
| NG_013358.2:g.4850C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_935918.1:n.73+30G>T | ||
| XR_935919.1:n.72+26G>T | ||
| XR_001754035.2:n.81+30G>T | ||
| XR_935918.2:n.81+30G>T |