Canonical Allele Identifier:
CA2581790032
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.126573377T>A , CM000664.2:g.126573377T>A | GRCh38 |
| NC_000002.11:g.127330954T>A , CM000664.1:g.127330954T>A | GRCh37 |
| NC_000002.10:g.127047424T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011512267.1:c.403-36860A>T | XP_011510569.1:n.403-36860A>T | |
| XR_001739693.1:n.211-36860A>T |