Linked Data
dbSNP Id:
rs1803414180
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.141973929T>C , CM000669.2:g.141973929T>C | GRCh38 |
| NC_000007.13:g.141673729T>C , CM000669.1:g.141673729T>C | GRCh37 |
| NC_000007.12:g.141320198T>C | NCBI36 |
| NG_016141.1:g.4845A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000465654.5:c.-3+27932T>C (MGAM) | ENSP00000419372.1:n.-3+27932T>C | |
| XM_011515783.1:c.*25-12467T>C (OR9A4) | XP_011514085.1:n.*25-12467T>C |