Canonical Allele Identifier:
CA2706388947
Gene:
Linked Data
dbSNP Id:
rs2110343166
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.74304473C>T , CM000666.2:g.74304473C>T | GRCh38 |
| NC_000004.11:g.75170190C>T , CM000666.1:g.75170190C>T | GRCh37 |
| NC_000004.10:g.75389054C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_938877.1:n.120-25695G>A | ||
| XR_938877.2:n.126-25695G>A |