Linked Data
dbSNP Id:
rs116645643
gnomAD v2:
3-133319878-T-C
gnomAD v3:
3-133601034-T-C
gnomAD v4:
3-133601034-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.133601034T>C , CM000665.2:g.133601034T>C | GRCh38 |
| NC_000003.11:g.133319878T>C , CM000665.1:g.133319878T>C | GRCh37 |
| NC_000003.10:g.134802568T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000260810.10:c.*216A>G MANE Select | ENSP00000260810.5:n.*216A>G | |
| ENST00000642236.1:c.*216A>G | ENSP00000493612.1:n.*216A>G | |
| ENST00000260810.9:c.*216A>G | ENSP00000260810.5:n.*216A>G | |
| ENST00000503338.5:n.163-2404A>G | ||
| ENST00000503464.1:n.163-2404A>G | ||
| NM_007027.3:c.*216A>G | NP_008958.2:n.*216A>G | |
| XM_005247076.2:c.*216A>G | XP_005247133.1:n.*216A>G | |
| NM_001363889.1:c.*216A>G | NP_001350818.1:n.*216A>G | |
| XM_017005636.2:c.*216A>G | XP_016861125.1:n.*216A>G | |
| XM_017005637.2:c.*216A>G | XP_016861126.1:n.*216A>G | |
| XR_001739988.2:n.4813A>G | ||
| NM_001363889.2:c.*216A>G | NP_001350818.1:n.*216A>G | |
| NM_007027.4:c.*216A>G MANE Select | NP_008958.2:n.*216A>G |