Canonical Allele Identifier:
CA2249826784
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.15922707A= , CM000679.2:g.15922707A= | GRCh38 |
| NC_000017.10:g.15826021A= , CM000679.1:g.15826021A= | GRCh37 |
| NC_000017.9:g.15766746A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XM_011524118.1:c.349-3436A= | XP_011522420.1:n.349-3436A= |