Canonical Allele Identifier:
CA1027923142
Gene:
Linked Data
dbSNP Id:
rs1664550967
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.16458150A>T , CM000664.2:g.16458150A>T | GRCh38 |
| NC_000002.11:g.16639418A>T , CM000664.1:g.16639418A>T | GRCh37 |
| NC_000002.10:g.16502899A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_939752.1:n.396-3056T>A |