Linked Data
ClinVar Variation Id:
5849
dbSNP Id:
rs121908450
ExAC:
2:109545744 C / T
gnomAD v2:
2-109545744-C-T
gnomAD v3:
2-108929288-C-T
gnomAD v4:
2-108929288-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.108929288C>T , CM000664.2:g.108929288C>T | GRCh38 |
| NC_000002.11:g.109545744C>T , CM000664.1:g.109545744C>T | GRCh37 |
| NC_000002.10:g.108912176C>T | NCBI36 |
| NG_008257.1:g.65085G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258443.7:c.266G>A (EDAR) MANE Select | ENSP00000258443.2:p.Arg89His | |
| ENST00000258443.6:c.266G>A (EDAR) | ENSP00000258443.2:p.Arg89His | |
| ENST00000376651.1:c.266G>A (EDAR) | ENSP00000365839.1:p.Arg89His | |
| ENST00000409271.5:c.266G>A (EDAR) | ENSP00000386371.1:p.Arg89His | |
| NM_022336.3:c.266G>A (EDAR) | NP_071731.1:p.Arg89His | |
| XM_006712204.1:c.266G>A (EDAR) | XP_006712267.1:p.Arg89His | |
| XM_011510502.1:c.317G>A (EDAR) | XP_011508804.1:p.Arg106His | |
| XM_011510503.1:c.317G>A (EDAR) | XP_011508805.1:p.Arg106His | |
| XM_011510502.2:c.410G>A (EDAR) | XP_011508804.2:p.Arg137His | |
| XM_011510503.2:c.410G>A (EDAR) | XP_011508805.2:p.Arg137His | |
| XM_017004623.2:c.8370+156242C>T (RANBP2) | XP_016860112.1:n.8370+156242C>T | |
| NM_022336.4:c.266G>A (EDAR) MANE Select | NP_071731.1:p.Arg89His |