Linked Data
MyVariant Identifiers:
chr12:g.55916774T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.55522990T>A , CM000674.2:g.55522990T>A | GRCh38 |
| NC_000012.11:g.55916774T>A , CM000674.1:g.55916774T>A | GRCh37 |
| NC_000012.10:g.54203041T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000419708.1:n.398T>A (OR6C64P) | ||
| XM_011538339.1:c.-147-29832A>T (OR6C70) | XP_011536641.1:n.-147-29832A>T | |
| XM_011538340.1:c.-147-29832A>T (OR6C70) | XP_011536642.1:n.-147-29832A>T | |
| XM_011538341.1:c.-147-29832A>T (OR6C70) | XP_011536643.1:n.-147-29832A>T |