Linked Data
gnomAD v4:
7-141973822-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.141973822C>G , CM000669.2:g.141973822C>G | GRCh38 |
| NC_000007.13:g.141673622C>G , CM000669.1:g.141673622C>G | GRCh37 |
| NC_000007.12:g.141320091C>G | NCBI36 |
| NG_016141.1:g.4952G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000465654.5:c.-3+27825C>G (MGAM) | ENSP00000419372.1:n.-3+27825C>G | |
| XM_011515783.1:c.*25-12574C>G (OR9A4) | XP_011514085.1:n.*25-12574C>G |