Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.141973814A>T , CM000669.2:g.141973814A>T | GRCh38 |
| NC_000007.13:g.141673614A>T , CM000669.1:g.141673614A>T | GRCh37 |
| NC_000007.12:g.141320083A>T | NCBI36 |
| NG_016141.1:g.4960T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000465654.5:c.-3+27817A>T (MGAM) | ENSP00000419372.1:n.-3+27817A>T | |
| XM_011515783.1:c.*25-12582A>T (OR9A4) | XP_011514085.1:n.*25-12582A>T |