Linked Data
dbSNP Id:
rs936553800
gnomAD v3:
7-141973809-A-G
gnomAD v4:
7-141973809-A-G
MyVariant Identifiers:
chr7:g.141973809A>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.141973809A>G , CM000669.2:g.141973809A>G | GRCh38 |
| NC_000007.13:g.141673609A>G , CM000669.1:g.141673609A>G | GRCh37 |
| NC_000007.12:g.141320078A>G | NCBI36 |
| NG_016141.1:g.4965T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000465654.5:c.-3+27812A>G (MGAM) | ENSP00000419372.1:n.-3+27812A>G | |
| XM_011515783.1:c.*25-12587A>G (OR9A4) | XP_011514085.1:n.*25-12587A>G |