Linked Data
ClinVar Variation Id:
266030
ClinVar RCV Id:
RCV000256441
dbSNP Id:
rs766858016
gnomAD v4:
2-25247710-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.25247710T>G , CM000664.2:g.25247710T>G | GRCh38 |
| NC_000002.11:g.25470579T>G , CM000664.1:g.25470579T>G | GRCh37 |
| NC_000002.10:g.25324083T>G | NCBI36 |
| NG_029465.2:g.99881A>C , LRG_459:g.99881A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000683393.1:c.1A>C | ENSP00000508654.1:p.Lys1Gln | |
| ENST00000683760.1:c.226A>C | ENSP00000507765.1:p.Lys76Gln | |
| ENST00000321117.10:c.895A>C MANE Select | ENSP00000324375.5:p.Lys299Gln | |
| ENST00000264709.7:c.895A>C | ENSP00000264709.3:p.Lys299Gln | |
| ENST00000321117.9:c.895A>C | ENSP00000324375.5:p.Lys299Gln | |
| ENST00000380746.8:c.328A>C | ENSP00000370122.4:p.Lys110Gln | |
| ENST00000380756.7:c.895A>C | ENSP00000370132.3:p.Lys299Gln | |
| ENST00000402667.1:c.226A>C | ENSP00000384237.1:p.Lys76Gln | |
| ENST00000470983.5:n.342A>C | ||
| ENST00000474807.5:n.190A>C | ||
| ENST00000496570.1:n.428A>C | ||
| NM_022552.4:c.895A>C , LRG_459t1:c.895A>C | NP_072046.2:p.Lys299Gln | |
| NM_153759.3:c.328A>C , LRG_459t2:c.328A>C | NP_715640.2:p.Lys110Gln | |
| NM_175629.2:c.895A>C , LRG_459t4:c.895A>C | NP_783328.1:p.Lys299Gln | |
| XM_005264175.3:c.895A>C | XP_005264232.1:p.Lys299Gln | |
| XM_005264177.3:c.226A>C | XP_005264234.1:p.Lys76Gln | |
| XM_006711957.2:c.895A>C | XP_006712020.1:p.Lys299Gln | |
| XM_006711958.2:c.451A>C | XP_006712021.1:p.Lys151Gln | |
| XM_011532662.1:c.748A>C | XP_011530964.1:p.Lys250Gln | |
| XM_011532663.1:c.730A>C | XP_011530965.1:p.Lys244Gln | |
| XM_011532664.1:c.895A>C | XP_011530966.1:p.Lys299Gln | |
| XM_011532665.1:c.439A>C | XP_011530967.1:p.Lys147Gln | |
| XM_011532666.1:c.367A>C | XP_011530968.1:p.Lys123Gln | |
| XM_011532667.1:c.226A>C | XP_011530969.1:p.Lys76Gln | |
| XM_011532668.1:c.895A>C | XP_011530970.1:p.Lys299Gln | |
| NM_001320893.1:c.439A>C | NP_001307822.1:p.Lys147Gln | |
| NR_135490.1:n.1233A>C | ||
| XM_005264175.5:c.895A>C | XP_005264232.1:p.Lys299Gln | |
| XM_005264177.4:c.226A>C | XP_005264234.1:p.Lys76Gln | |
| XM_011532662.2:c.748A>C | XP_011530964.1:p.Lys250Gln | |
| XM_011532663.2:c.730A>C | XP_011530965.1:p.Lys244Gln | |
| XM_011532664.2:c.895A>C | XP_011530966.1:p.Lys299Gln | |
| XM_011532666.2:c.367A>C | XP_011530968.1:p.Lys123Gln | |
| XM_011532667.3:c.226A>C | XP_011530969.1:p.Lys76Gln | |
| XM_017003526.1:c.895A>C | XP_016859015.1:p.Lys299Gln | |
| XM_017003527.1:c.226A>C | XP_016859016.1:p.Lys76Gln | |
| XR_001738657.1:n.1172A>C | ||
| NM_001375819.1:c.226A>C | NP_001362748.1:p.Lys76Gln | |
| NR_135490.2:n.1126A>C | ||
| NM_022552.5:c.895A>C MANE Select | NP_072046.2:p.Lys299Gln |