Linked Data
dbSNP Id:
rs2120814884
gnomAD v4:
12-55522943-C-T
MyVariant Identifiers:
chr12:g.55916727C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.55522943C>T , CM000674.2:g.55522943C>T | GRCh38 |
| NC_000012.11:g.55916727C>T , CM000674.1:g.55916727C>T | GRCh37 |
| NC_000012.10:g.54202994C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000419708.1:n.351C>T (OR6C64P) | ||
| XM_011538339.1:c.-147-29785G>A (OR6C70) | XP_011536641.1:n.-147-29785G>A | |
| XM_011538340.1:c.-147-29785G>A (OR6C70) | XP_011536642.1:n.-147-29785G>A | |
| XM_011538341.1:c.-147-29785G>A (OR6C70) | XP_011536643.1:n.-147-29785G>A |