Canonical Allele Identifier:
CA2051430548
Gene:
Linked Data
dbSNP Id:
rs1874808558
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.84952226C>T , CM000674.2:g.84952226C>T | GRCh38 |
| NC_000012.11:g.85346005C>T , CM000674.1:g.85346005C>T | GRCh37 |
| NC_000012.10:g.83870136C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_945152.1:n.316+30912C>T | ||
| XR_945153.1:n.301+13762C>T | ||
| XR_945154.1:n.175-36716C>T | ||
| XR_945155.1:n.330+30912C>T | ||
| XR_945152.2:n.316+30912C>T | ||
| XR_945154.2:n.175-36716C>T | ||
| XR_945155.2:n.888+30912C>T |