Canonical Allele Identifier:
CA1202461550
Gene:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160776286G>C , CM000663.2:g.160776286G>C | GRCh38 |
| NC_000001.10:g.160746076G>C , CM000663.1:g.160746076G>C | GRCh37 |
| NC_000001.9:g.159012700G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000620690.1:n.262+61C>G | ||
| XR_922204.1:n.447C>G | ||
| XR_922205.1:n.414+33C>G | ||
| XR_922206.1:n.447C>G | ||
| XR_001738267.1:n.430+33C>G | ||
| XR_922205.2:n.430+33C>G |