Canonical Allele Identifier:
CA1677169882
Gene:
Linked Data
dbSNP Id:
rs1780347715
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.160668472T>A , CM000668.2:g.160668472T>A | GRCh38 |
| NC_000006.11:g.161089504T>A , CM000668.1:g.161089504T>A | GRCh37 |
| NC_000006.10:g.161009494T>A | NCBI36 |
| NG_016147.1:g.2904A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452651.1:n.115-2099A>T |