Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.141973922C= , CM000669.2:g.141973922C= | GRCh38 |
| NC_000007.13:g.141673722C= , CM000669.1:g.141673722C= | GRCh37 |
| NC_000007.12:g.141320191C= | NCBI36 |
| NG_016141.1:g.4852G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000465654.5:c.-3+27925C= (MGAM) | ENSP00000419372.1:n.-3+27925C= | |
| XM_011515783.1:c.*25-12474C= (OR9A4) | XP_011514085.1:n.*25-12474C= |