Linked Data
dbSNP Id:
rs1028908296
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.40097254T>C , CM000663.2:g.40097254T>C | GRCh38 |
| NC_000001.10:g.40562926T>C , CM000663.1:g.40562926T>C | GRCh37 |
| NC_000001.9:g.40335513T>C | NCBI36 |
| NG_009192.1:g.5217A>G , LRG_690:g.5217A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000449045.7:c.-16A>G | ENSP00000392293.2:n.-16A>G | |
| ENST00000641319.1:c.-16A>G | ENSP00000493128.1:n.-16A>G | |
| ENST00000641691.1:c.-16A>G | ENSP00000492910.1:n.-16A>G | |
| ENST00000433473.7:c.-16A>G | ENSP00000394863.3:n.-16A>G | |
| NM_000310.3:c.-16A>G , LRG_690t1:c.-16A>G | NP_000301.1:n.-16A>G | |
| NM_001142604.1:c.-16A>G | NP_001136076.1:n.-16A>G | |
| XM_005271008.1:c.-16A>G | XP_005271065.1:n.-16A>G | |
| NM_001363695.1:c.-16A>G | NP_001350624.1:n.-16A>G |