Canonical Allele Identifier:
CA12283655
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.159085568C>T , CM000668.2:g.159085568C>T | GRCh38 |
| NC_000006.11:g.159506600C>T , CM000668.1:g.159506600C>T | GRCh37 |
| NC_000006.10:g.159426588C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011536288.1:c.323+10161G>A | XP_011534590.1:n.323+10161G>A | |
| XM_011536289.1:c.209+10161G>A | XP_011534591.1:n.209+10161G>A | |
| XM_024446608.1:c.323+10161G>A | XP_024302376.1:n.323+10161G>A |