Canonical Allele Identifier:
CA657091012
Gene:
Linked Data
COSMIC:
COSN19411683
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.20218126T>C , CM000681.2:g.20218126T>C | GRCh38 |
| NC_000019.9:g.20328935T>C , CM000681.1:g.20328935T>C | GRCh37 |
| NC_000019.8:g.20189935T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_936388.1:n.619-810A>G | ||
| XR_936389.1:n.502-810A>G | ||
| XR_936390.1:n.511-810A>G | ||
| XR_936391.1:n.514-810A>G | ||
| XR_936392.1:n.514-810A>G | ||
| XR_936394.1:n.41-608T>C | ||
| XR_001754063.2:n.1506-810A>G | ||
| XR_001754064.2:n.138-810A>G | ||
| XR_001754066.1:n.3912-810A>G | ||
| XR_001754067.1:n.3912-810A>G | ||
| XR_001754068.1:n.3912-810A>G | ||
| XR_936394.2:n.41-608T>C | ||
| XR_936406.2:n.1411-810A>G |