Canonical Allele Identifier:
CA1672979078
Gene:
Linked Data
dbSNP Id:
rs1777186014
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.151633559T>C , CM000668.2:g.151633559T>C | GRCh38 |
| NC_000006.11:g.151954694T>C , CM000668.1:g.151954694T>C | GRCh37 |
| NC_000006.10:g.151996387T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_943115.1:n.2496+3577T>C |