Linked Data
ClinVar Variation Id:
8901
dbSNP Id:
rs137852697
ExAC:
1:40557843 T / C
gnomAD v2:
1-40557843-T-C
gnomAD v4:
1-40092171-T-C
PubMed:
PMID:9425237
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.40092171T>C , CM000663.2:g.40092171T>C | GRCh38 |
| NC_000001.10:g.40557843T>C , CM000663.1:g.40557843T>C | GRCh37 |
| NC_000001.9:g.40330430T>C | NCBI36 |
| NG_009192.1:g.10300A>G , LRG_690:g.10300A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372779.9:c.*72A>G | ENSP00000361865.5:n.*72A>G | |
| ENST00000433473.8:c.233A>G | ENSP00000394863.4:p.Asp78Gly | |
| ENST00000439754.6:c.236A>G | ENSP00000403207.2:p.Asp79Gly | |
| ENST00000449045.7:c.125-2659A>G | ENSP00000392293.2:n.125-2659A>G | |
| ENST00000526547.2:c.516A>G | ||
| ENST00000527311.7:c.234+227A>G | ENSP00000436695.3:n.234+227A>G | |
| ENST00000530704.6:c.236A>G | ENSP00000431655.1:p.Asp79Gly | |
| ENST00000641083.1:c.214A>G | ||
| ENST00000641236.1:n.473A>G | ||
| ENST00000641319.1:c.236A>G | ENSP00000493128.1:p.Asp79Gly | |
| ENST00000641471.1:c.323A>G | ENSP00000493146.1:p.Asp108Gly | |
| ENST00000641548.1:c.*88A>G | ENSP00000492984.1:n.*88A>G | |
| ENST00000641691.1:c.*88A>G | ENSP00000492910.1:n.*88A>G | |
| ENST00000641924.1:c.124+4944A>G | ENSP00000493063.1:n.124+4944A>G | |
| ENST00000642050.2:c.236A>G MANE Select | ENSP00000493153.1:p.Asp79Gly | |
| ENST00000372779.8:c.323A>G | ENSP00000361865.4:p.Asp108Gly | |
| ENST00000433473.7:c.236A>G | ENSP00000394863.3:p.Asp79Gly | |
| ENST00000449045.6:c.125-2659A>G | ENSP00000392293.2:n.125-2659A>G | |
| ENST00000526547.1:c.86A>G | ENSP00000436481.1:p.Asp29Gly | |
| ENST00000527311.6:c.125-114A>G | ENSP00000436695.2:n.125-114A>G | |
| ENST00000529905.5:c.236A>G | ENSP00000432053.1:p.Asp79Gly | |
| ENST00000530704.5:c.236A>G | ENSP00000431655.1:p.Asp79Gly | |
| NM_000310.3:c.236A>G , LRG_690t1:c.236A>G | NP_000301.1:p.Asp79Gly | |
| NM_001142604.1:c.125-2659A>G | NP_001136076.1:n.125-2659A>G | |
| XM_005271008.1:c.236A>G | XP_005271065.1:p.Asp79Gly | |
| NM_001363695.1:c.236A>G | NP_001350624.1:p.Asp79Gly | |
| NM_000310.4:c.236A>G MANE Select | NP_000301.1:p.Asp79Gly | |
| NM_001142604.2:c.125-2659A>G | NP_001136076.1:n.125-2659A>G | |
| NM_001363695.2:c.236A>G | NP_001350624.1:p.Asp79Gly |