Canonical Allele Identifier:
CA1025451875
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.36129905G>C , CM000684.2:g.36129905G>C | GRCh38 |
| NC_000022.10:g.36525953G>C , CM000684.1:g.36525953G>C | GRCh37 |
| NC_000022.9:g.34855899G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_430441.2:n.1547+3257C>G | ||
| XR_938219.1:n.3031C>G | ||
| XR_938220.1:n.3031C>G | ||
| XR_938221.1:n.1471+3957C>G | ||
| XR_001755516.2:n.4893C>G | ||
| XR_001755517.2:n.3120C>G | ||
| XR_001755518.2:n.4893C>G | ||
| XR_001755519.2:n.4893C>G | ||
| XR_001755520.2:n.4893C>G | ||
| XR_001755521.2:n.4893C>G | ||
| XR_001755522.2:n.1637-2132C>G | ||
| XR_001755525.2:n.1637-551C>G | ||
| XR_001755526.2:n.1637-2132C>G | ||
| XR_430441.4:n.1636+3257C>G |