Linked Data
ClinVar Variation Id:
65580
dbSNP Id:
rs112534524
ExAC:
4:110681527 C / T
gnomAD v2:
4-110681527-C-T
gnomAD v3:
4-109760371-C-T
gnomAD v4:
4-109760371-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.109760371C>T , CM000666.2:g.109760371C>T | GRCh38 |
| NC_000004.11:g.110681527C>T , CM000666.1:g.110681527C>T | GRCh37 |
| NC_000004.10:g.110900976C>T | NCBI36 |
| NG_007569.1:g.46615G>A , LRG_48:g.46615G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000695844.1:n.961G>A | ||
| ENST00000695845.1:n.960G>A | ||
| ENST00000695846.1:n.782G>A | ||
| ENST00000394634.7:c.782G>A MANE Select | ENSP00000378130.2:p.Gly261Asp | |
| ENST00000394635.8:c.782G>A | ENSP00000378131.3:p.Gly261Asp | |
| ENST00000645635.1:c.782G>A | ENSP00000493607.1:p.Gly261Asp | |
| ENST00000394634.6:c.782G>A | ENSP00000378130.2:p.Gly261Asp | |
| ENST00000394635.7:c.782G>A | ENSP00000378131.3:p.Gly261Asp | |
| ENST00000504853.3:n.1199G>A | ||
| ENST00000512148.5:c.782G>A | ENSP00000427438.1:p.Gly261Asp | |
| ENST00000618244.4:c.782G>A | ENSP00000483416.1:p.Gly261Asp | |
| NM_000204.3:c.782G>A , LRG_48t1:c.782G>A | NP_000195.2:p.Gly261Asp | |
| XM_005262975.1:c.782G>A | XP_005263032.1:p.Gly261Asp | |
| XM_005262976.1:c.782G>A | XP_005263033.1:p.Gly261Asp | |
| XM_006714209.1:c.782G>A | XP_006714272.1:p.Gly261Asp | |
| XM_006714210.2:c.782G>A | XP_006714273.1:p.Gly261Asp | |
| XM_011531920.1:c.782G>A | XP_011530222.1:p.Gly261Asp | |
| NM_000204.4:c.782G>A | NP_000195.2:p.Gly261Asp | |
| NM_001318057.1:c.782G>A | NP_001304986.1:p.Gly261Asp | |
| NM_001331035.1:c.782G>A | NP_001317964.1:p.Gly261Asp | |
| XM_006714210.4:c.782G>A | XP_006714273.1:p.Gly261Asp | |
| XM_011531920.2:c.782G>A | XP_011530222.1:p.Gly261Asp | |
| XM_017008164.2:c.782G>A | XP_016863653.1:p.Gly261Asp | |
| XM_017008165.2:c.782G>A | XP_016863654.1:p.Gly261Asp | |
| XM_017008166.2:c.782G>A | XP_016863655.1:p.Gly261Asp | |
| NM_001318057.2:c.782G>A | NP_001304986.2:p.Gly261Asp | |
| NM_001331035.2:c.782G>A | NP_001317964.1:p.Gly261Asp | |
| NM_001375278.1:c.782G>A | NP_001362207.1:p.Gly261Asp | |
| NM_001375279.1:c.782G>A | NP_001362208.1:p.Gly261Asp | |
| NM_001375280.1:c.782G>A | NP_001362209.1:p.Gly261Asp | |
| NM_001375281.1:c.782G>A | NP_001362210.1:p.Gly261Asp | |
| NM_001375282.1:c.782G>A | NP_001362211.1:p.Gly261Asp | |
| NM_001375283.1:c.782G>A | NP_001362212.1:p.Gly261Asp | |
| NM_001375284.1:c.173G>A | NP_001362213.1:p.Gly58Asp | |
| NR_164671.1:n.810G>A | ||
| NR_164672.1:n.810G>A | ||
| NR_164673.1:n.810G>A | ||
| NM_000204.5:c.782G>A MANE Select | NP_000195.3:p.Gly261Asp |