Linked Data
ClinVar Variation Id:
92910
dbSNP Id:
rs398123355
gnomAD v2:
3-33107026-A-C
gnomAD v3:
3-33065534-A-C
gnomAD v4:
3-33065534-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.33065534A>C , CM000665.2:g.33065534A>C | GRCh38 |
| NC_000003.11:g.33107026A>C , CM000665.1:g.33107026A>C | GRCh37 |
| NC_000003.10:g.33082030A>C | NCBI36 |
| NG_009005.1:g.36669T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307363.10:c.481T>G MANE Select | ENSP00000306920.4:p.Trp161Gly | |
| ENST00000307363.9:c.481T>G | ENSP00000306920.4:p.Trp161Gly | |
| ENST00000307377.12:c.269T>G | ENSP00000305920.8:p.Val90Gly | |
| ENST00000399402.7:c.391T>G | ENSP00000382333.2:p.Trp131Gly | |
| ENST00000415454.1:c.76-7265T>G | ENSP00000411813.1:n.76-7265T>G | |
| ENST00000438227.1:c.99T>G | ENSP00000401250.1:p.Ser33Arg | |
| ENST00000440656.1:c.88T>G | ENSP00000411769.1:p.Trp30Gly | |
| ENST00000446732.5:c.179T>G | ENSP00000407365.1:p.Val60Gly | |
| ENST00000464355.1:n.439T>G | ||
| ENST00000482097.5:n.109-11985T>G | ||
| ENST00000485698.5:n.137-11985T>G | ||
| ENST00000498537.5:n.133-11985T>G | ||
| NM_000404.2:c.481T>G | NP_000395.2:p.Trp161Gly | |
| NM_000404.3:c.481T>G | NP_000395.2:p.Trp161Gly | |
| NM_001079811.1:c.391T>G | NP_001073279.1:p.Trp131Gly | |
| NM_001079811.2:c.391T>G | NP_001073279.1:p.Trp131Gly | |
| NM_001135602.1:c.269T>G | NP_001129074.1:p.Val90Gly | |
| NM_001135602.2:c.269T>G | NP_001129074.1:p.Val90Gly | |
| NM_001317040.1:c.625T>G | NP_001303969.1:p.Trp209Gly | |
| NM_000404.4:c.481T>G MANE Select | NP_000395.3:p.Trp161Gly | |
| NM_001079811.3:c.391T>G | NP_001073279.2:p.Trp131Gly | |
| NM_001135602.3:c.269T>G | NP_001129074.2:p.Val90Gly | |
| NM_001317040.2:c.625T>G | NP_001303969.2:p.Trp209Gly | |
| NM_001393580.1:c.481T>G | NP_001380509.1:p.Trp161Gly |