Canonical Allele Identifier:
CA2221608958
Gene:
Linked Data
dbSNP Id:
rs907426825
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.50109050A>C , CM000678.2:g.50109050A>C | GRCh38 |
| NC_000016.9:g.50142961A>C , CM000678.1:g.50142961A>C | GRCh37 |
| NC_000016.8:g.48700462A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011523490.1:c.115-2398T>G | XP_011521792.1:n.115-2398T>G |