Linked Data
ClinVar Variation Id:
365361
dbSNP Id:
rs886063555
gnomAD v2:
9-135203868-T-C
gnomAD v3:
9-132328481-T-C
gnomAD v4:
9-132328481-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.132328481T>C , CM000671.2:g.132328481T>C | GRCh38 |
| NC_000009.11:g.135203868T>C , CM000671.1:g.135203868T>C | GRCh37 |
| NC_000009.10:g.134193689T>C | NCBI36 |
| NG_007946.1:g.31505A>G , LRG_268:g.31505A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000224140.6:c.3117A>G MANE Select | ENSP00000224140.5:p.Ile1039Met | |
| ENST00000224140.5:c.3117A>G | ENSP00000224140.5:p.Ile1039Met | |
| NM_015046.5:c.3117A>G , LRG_268t1:c.3117A>G | NP_055861.3:p.Ile1039Met | |
| XM_005272171.1:c.3117A>G | XP_005272228.1:p.Ile1039Met | |
| XM_005272172.1:c.3117A>G | XP_005272229.1:p.Ile1039Met | |
| XM_005272173.1:c.3117A>G | XP_005272230.1:p.Ile1039Met | |
| XM_011518404.1:c.3117A>G | XP_011516706.1:p.Ile1039Met | |
| XM_011518405.1:c.3117A>G | XP_011516707.1:p.Ile1039Met | |
| XM_011518406.1:c.3117A>G | XP_011516708.1:p.Ile1039Met | |
| XM_011518407.1:c.3117A>G | XP_011516709.1:p.Ile1039Met | |
| XM_011518408.1:c.3117A>G | XP_011516710.1:p.Ile1039Met | |
| XR_929739.1:n.3301A>G | ||
| NM_001351527.1:c.3117A>G | NP_001338456.1:p.Ile1039Met | |
| NM_001351528.1:c.3117A>G | NP_001338457.1:p.Ile1039Met | |
| NM_015046.6:c.3117A>G | NP_055861.3:p.Ile1039Met | |
| XM_005272172.3:c.3117A>G | XP_005272229.1:p.Ile1039Met | |
| XM_005272173.3:c.3117A>G | XP_005272230.1:p.Ile1039Met | |
| XM_011518404.3:c.3117A>G | XP_011516706.1:p.Ile1039Met | |
| XM_011518405.3:c.3117A>G | XP_011516707.1:p.Ile1039Met | |
| XM_011518406.2:c.3117A>G | XP_011516708.1:p.Ile1039Met | |
| XM_011518408.3:c.3117A>G | XP_011516710.1:p.Ile1039Met | |
| XR_001746251.1:n.3301A>G | ||
| XR_929739.2:n.3301A>G | ||
| NM_015046.7:c.3117A>G MANE Select | NP_055861.3:p.Ile1039Met | |
| NM_001351528.2:c.3117A>G | NP_001338457.1:p.Ile1039Met | |
| NM_001351527.2:c.3117A>G | NP_001338456.1:p.Ile1039Met |