Canonical Allele Identifier:
CA1818149976
Gene:
Linked Data
dbSNP Id:
rs1814940112
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.126999817T>C , CM000670.2:g.126999817T>C | GRCh38 |
| NC_000008.10:g.128012062T>C , CM000670.1:g.128012062T>C | GRCh37 |
| NC_000008.9:g.128081244T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001746076.2:n.1301-6738T>C |