Canonical Allele Identifier:
CA1674885612
Gene:
Linked Data
dbSNP Id:
rs1778855129
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.155812395C>T , CM000668.2:g.155812395C>T | GRCh38 |
| NC_000006.11:g.156133529C>T , CM000668.1:g.156133529C>T | GRCh37 |
| NC_000006.10:g.156175221C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_943142.1:n.79+18976C>T | ||
| XR_943146.1:n.645-356G>A | ||
| XR_001744423.1:n.699-356G>A | ||
| XR_001744424.1:n.79+18976C>T |