Canonical Allele Identifier:
CA2701396652
Gene:
Linked Data
dbSNP Id:
rs2105755367
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.200033363T>C , CM000664.2:g.200033363T>C | GRCh38 |
| NC_000002.11:g.200898086T>C , CM000664.1:g.200898086T>C | GRCh37 |
| NC_000002.10:g.200606331T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923778.1:n.178-22467A>G |