Canonical Allele Identifier:
CA2838210496
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.43066764C>T , CM000664.2:g.43066764C>T | GRCh38 |
| NC_000002.11:g.43293902C>T , CM000664.1:g.43293902C>T | GRCh37 |
| NC_000002.10:g.43147406C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_017005459.1:c.*493-57G>A | XP_016860948.1:n.*493-57G>A | |
| XM_017005460.1:c.*493-215G>A | XP_016860949.1:n.*493-215G>A |