Canonical Allele Identifier:
CA1605794996
Gene:
Linked Data
dbSNP Id:
rs1761315381
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.1535578G>C , CM000668.2:g.1535578G>C | GRCh38 |
| NC_000006.11:g.1535813G>C , CM000668.1:g.1535813G>C | GRCh37 |
| NC_000006.10:g.1480812G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_427861.2:n.234+16768C>G | ||
| XR_926380.1:n.218-2878G>C | ||
| XR_926381.1:n.1108-2878G>C | ||
| XR_926382.1:n.235-6399C>G | ||
| XR_926384.1:n.200-6399C>G | ||
| XR_001743921.1:n.235-6423C>G | ||
| XR_427861.3:n.234+16768C>G | ||
| XR_926381.2:n.1123-2878G>C |