Linked Data
dbSNP Id:
rs11760281
gnomAD v2:
7-80104549-A-G
gnomAD v3:
7-80475233-A-G
gnomAD v4:
7-80475233-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.80475233A>G , CM000669.2:g.80475233A>G | GRCh38 |
| NC_000007.13:g.80104549A>G , CM000669.1:g.80104549A>G | GRCh37 |
| NC_000007.12:g.79942485A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000398291.4:c.462-854T>C (GNAT3) MANE Select | ENSP00000381339.3:n.462-854T>C | |
| ENST00000398291.3:c.462-854T>C (GNAT3) | ENSP00000381339.3:n.462-854T>C | |
| ENST00000435819.5:c.-477-11234A>G (CD36) | ENSP00000399421.1:n.-477-11234A>G | |
| NM_001102386.1:c.462-854T>C (GNAT3) | NP_001095856.1:n.462-854T>C | |
| XM_011516123.1:c.462-854T>C (GNAT3) | XP_011514425.1:n.462-854T>C | |
| XM_011516124.1:c.462-854T>C (GNAT3) | XP_011514426.1:n.462-854T>C | |
| XM_011516125.1:c.171-854T>C (GNAT3) | XP_011514427.1:n.171-854T>C | |
| NM_001102386.2:c.462-854T>C (GNAT3) | NP_001095856.1:n.462-854T>C | |
| XM_011516124.2:c.462-854T>C (GNAT3) | XP_011514426.1:n.462-854T>C | |
| NM_001102386.3:c.462-854T>C (GNAT3) MANE Select | NP_001095856.1:n.462-854T>C |