Canonical Allele Identifier:
CA2713322816
Gene:
Linked Data
dbSNP Id:
rs2114700373
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.155817695G>T , CM000668.2:g.155817695G>T | GRCh38 |
| NC_000006.11:g.156138829G>T , CM000668.1:g.156138829G>T | GRCh37 |
| NC_000006.10:g.156180521G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_943142.1:n.79+24276G>T | ||
| XR_943146.1:n.552-3025C>A | ||
| XR_001744423.1:n.606-3025C>A | ||
| XR_001744424.1:n.79+24276G>T |