Linked Data
gnomAD v4:
7-141973899-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.141973899C>A , CM000669.2:g.141973899C>A | GRCh38 |
| NC_000007.13:g.141673699C>A , CM000669.1:g.141673699C>A | GRCh37 |
| NC_000007.12:g.141320168C>A | NCBI36 |
| NG_016141.1:g.4875G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000465654.5:c.-3+27902C>A (MGAM) | ENSP00000419372.1:n.-3+27902C>A | |
| XM_011515783.1:c.*25-12497C>A (OR9A4) | XP_011514085.1:n.*25-12497C>A |