Linked Data
MyVariant Identifiers:
chr12:g.55916732A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.55522948A>C , CM000674.2:g.55522948A>C | GRCh38 |
| NC_000012.11:g.55916732A>C , CM000674.1:g.55916732A>C | GRCh37 |
| NC_000012.10:g.54202999A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000419708.1:n.356A>C (OR6C64P) | ||
| XM_011538339.1:c.-147-29790T>G (OR6C70) | XP_011536641.1:n.-147-29790T>G | |
| XM_011538340.1:c.-147-29790T>G (OR6C70) | XP_011536642.1:n.-147-29790T>G | |
| XM_011538341.1:c.-147-29790T>G (OR6C70) | XP_011536643.1:n.-147-29790T>G |