Canonical Allele Identifier:
CA2706164630
Gene:
Linked Data
dbSNP Id:
rs904493030
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.74304435G>T , CM000666.2:g.74304435G>T | GRCh38 |
| NC_000004.11:g.75170152G>T , CM000666.1:g.75170152G>T | GRCh37 |
| NC_000004.10:g.75389016G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_938877.1:n.120-25657C>A | ||
| XR_938877.2:n.126-25657C>A |