Canonical Allele Identifier:
CA1674885851
Gene:
Linked Data
dbSNP Id:
rs1299005091
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.155812610G>A , CM000668.2:g.155812610G>A | GRCh38 |
| NC_000006.11:g.156133744G>A , CM000668.1:g.156133744G>A | GRCh37 |
| NC_000006.10:g.156175436G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_943142.1:n.79+19191G>A | ||
| XR_943146.1:n.645-571C>T | ||
| XR_001744423.1:n.699-571C>T | ||
| XR_001744424.1:n.79+19191G>A |