Linked Data
gnomAD v4:
7-141973857-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.141973857A>C , CM000669.2:g.141973857A>C | GRCh38 |
| NC_000007.13:g.141673657A>C , CM000669.1:g.141673657A>C | GRCh37 |
| NC_000007.12:g.141320126A>C | NCBI36 |
| NG_016141.1:g.4917T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000465654.5:c.-3+27860A>C (MGAM) | ENSP00000419372.1:n.-3+27860A>C | |
| XM_011515783.1:c.*25-12539A>C (OR9A4) | XP_011514085.1:n.*25-12539A>C |