Linked Data
dbSNP Id:
rs749473578
ExAC:
1:40557722 T / C
gnomAD v2:
1-40557722-T-C
gnomAD v3:
1-40092050-T-C
gnomAD v4:
1-40092050-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.40092050T>C , CM000663.2:g.40092050T>C | GRCh38 |
| NC_000001.10:g.40557722T>C , CM000663.1:g.40557722T>C | GRCh37 |
| NC_000001.9:g.40330309T>C | NCBI36 |
| NG_009192.1:g.10421A>G , LRG_690:g.10421A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372779.9:c.*193A>G | ENSP00000361865.5:n.*193A>G | |
| ENST00000433473.8:c.354A>G | ENSP00000394863.4:p.Gln118= | |
| ENST00000439754.6:c.357A>G | ENSP00000403207.2:p.Gln119= | |
| ENST00000449045.7:c.125-2538A>G | ENSP00000392293.2:n.125-2538A>G | |
| ENST00000526547.2:c.637A>G | ||
| ENST00000527311.7:c.234+348A>G | ENSP00000436695.3:n.234+348A>G | |
| ENST00000530704.6:c.357A>G | ENSP00000431655.1:p.Gln119= | |
| ENST00000641083.1:c.335A>G | ||
| ENST00000641236.1:n.594A>G | ||
| ENST00000641319.1:c.357A>G | ENSP00000493128.1:p.Gln119= | |
| ENST00000641471.1:c.444A>G | ENSP00000493146.1:p.Gln148= | |
| ENST00000641548.1:c.*209A>G | ENSP00000492984.1:n.*209A>G | |
| ENST00000641691.1:c.*209A>G | ENSP00000492910.1:n.*209A>G | |
| ENST00000641924.1:c.124+5065A>G | ENSP00000493063.1:n.124+5065A>G | |
| ENST00000642050.2:c.357A>G MANE Select | ENSP00000493153.1:p.Gln119= | |
| ENST00000372779.8:c.444A>G | ENSP00000361865.4:p.Gln148= | |
| ENST00000433473.7:c.357A>G | ENSP00000394863.3:p.Gln119= | |
| ENST00000439754.5:c.42A>G | ENSP00000403207.1:p.Gln14= | |
| ENST00000449045.6:c.125-2538A>G | ENSP00000392293.2:n.125-2538A>G | |
| ENST00000526547.1:c.207A>G | ENSP00000436481.1:p.Gln69= | |
| ENST00000527311.6:c.132A>G | ENSP00000436695.2:p.Gln44= | |
| ENST00000529905.5:c.357A>G | ENSP00000432053.1:p.Gln119= | |
| ENST00000530704.5:c.357A>G | ENSP00000431655.1:p.Gln119= | |
| NM_000310.3:c.357A>G , LRG_690t1:c.357A>G | NP_000301.1:p.Gln119= | |
| NM_001142604.1:c.125-2538A>G | NP_001136076.1:n.125-2538A>G | |
| XM_005271008.1:c.357A>G | XP_005271065.1:p.Gln119= | |
| NM_001363695.1:c.357A>G | NP_001350624.1:p.Gln119= | |
| NM_000310.4:c.357A>G MANE Select | NP_000301.1:p.Gln119= | |
| NM_001142604.2:c.125-2538A>G | NP_001136076.1:n.125-2538A>G | |
| NM_001363695.2:c.357A>G | NP_001350624.1:p.Gln119= |