Canonical Allele Identifier:
CA1677169996
Gene:
Linked Data
dbSNP Id:
rs1582912427
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.160668666T>G , CM000668.2:g.160668666T>G | GRCh38 |
| NC_000006.11:g.161089698T>G , CM000668.1:g.161089698T>G | GRCh37 |
| NC_000006.10:g.161009688T>G | NCBI36 |
| NG_016147.1:g.2710A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452651.1:n.115-2293A>C |