Linked Data
MyVariant Identifiers:
chr12:g.55916625G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.55522841G>T , CM000674.2:g.55522841G>T | GRCh38 |
| NC_000012.11:g.55916625G>T , CM000674.1:g.55916625G>T | GRCh37 |
| NC_000012.10:g.54202892G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000419708.1:n.249G>T (OR6C64P) | ||
| XM_011538339.1:c.-147-29683C>A (OR6C70) | XP_011536641.1:n.-147-29683C>A | |
| XM_011538340.1:c.-147-29683C>A (OR6C70) | XP_011536642.1:n.-147-29683C>A | |
| XM_011538341.1:c.-147-29683C>A (OR6C70) | XP_011536643.1:n.-147-29683C>A |