Canonical Allele Identifier:
CA1468682143
Gene:
Linked Data
dbSNP Id:
rs10034692
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.74554070A>T , CM000666.2:g.74554070A>T | GRCh38 |
| NC_000004.11:g.75419787A>T , CM000666.1:g.75419787A>T | GRCh37 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_001741513.1:n.167-1238T>A |