Canonical Allele Identifier:
CA1318169464
Gene:
Linked Data
dbSNP Id:
rs1688120398
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.195007061T>A , CM000664.2:g.195007061T>A | GRCh38 |
| NC_000002.11:g.195871785T>A , CM000664.1:g.195871785T>A | GRCh37 |
| NC_000002.10:g.195580030T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_001739836.1:n.553+52374A>T |