Canonical Allele Identifier:
CA1233617206
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.1554155T= , CM000664.2:g.1554155T= | GRCh38 |
| NC_000002.11:g.1557927T= , CM000664.1:g.1557927T= | GRCh37 |
| NC_000002.10:g.1536934T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NR_168373.1:n.746-15T= | |
| XM_011510447.1:c.-1018T= | XP_011508749.1:n.-1018T= |
| XM_011510448.1:c.-1018T= | XP_011508750.1:n.-1018T= |
| XM_017005455.1:c.-1018T= | XP_016860944.1:n.-1018T= |
| XR_922720.1:n.85+2343A= |