Canonical Allele Identifier:
CA1674890246
Gene:
Linked Data
dbSNP Id:
rs1778929168
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.155817630T>A , CM000668.2:g.155817630T>A | GRCh38 |
| NC_000006.11:g.156138764T>A , CM000668.1:g.156138764T>A | GRCh37 |
| NC_000006.10:g.156180456T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_943142.1:n.79+24211T>A | ||
| XR_943146.1:n.552-2960A>T | ||
| XR_001744423.1:n.606-2960A>T | ||
| XR_001744424.1:n.79+24211T>A |