Linked Data
dbSNP Id:
rs1873167987
gnomAD v4:
12-55522979-T-C
MyVariant Identifiers:
chr12:g.55916763T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.55522979T>C , CM000674.2:g.55522979T>C | GRCh38 |
| NC_000012.11:g.55916763T>C , CM000674.1:g.55916763T>C | GRCh37 |
| NC_000012.10:g.54203030T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000419708.1:n.387T>C (OR6C64P) | ||
| XM_011538339.1:c.-147-29821A>G (OR6C70) | XP_011536641.1:n.-147-29821A>G | |
| XM_011538340.1:c.-147-29821A>G (OR6C70) | XP_011536642.1:n.-147-29821A>G | |
| XM_011538341.1:c.-147-29821A>G (OR6C70) | XP_011536643.1:n.-147-29821A>G |