Canonical Allele Identifier:
CA1438624528
Gene:
Linked Data
dbSNP Id:
rs1713321299
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.11501970A>G , CM000666.2:g.11501970A>G | GRCh38 |
| NC_000004.11:g.11503594A>G , CM000666.1:g.11503594A>G | GRCh37 |
| NC_000004.10:g.11112692A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001741361.1:n.950+19124A>G |