Linked Data
dbSNP Id:
rs767752758
ExAC:
2:109513516 A / G
gnomAD v2:
2-109513516-A-G
gnomAD v4:
2-108897060-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.108897060A>G , CM000664.2:g.108897060A>G | GRCh38 |
| NC_000002.11:g.109513516A>G , CM000664.1:g.109513516A>G | GRCh37 |
| NC_000002.10:g.108879948A>G | NCBI36 |
| NG_008257.1:g.97313T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258443.7:c.1194T>C (EDAR) MANE Select | ENSP00000258443.2:p.Phe398= | |
| ENST00000258443.6:c.1194T>C (EDAR) | ENSP00000258443.2:p.Phe398= | |
| ENST00000376651.1:c.1290T>C (EDAR) | ENSP00000365839.1:p.Phe430= | |
| ENST00000409271.5:c.1290T>C (EDAR) | ENSP00000386371.1:p.Phe430= | |
| NM_022336.3:c.1194T>C (EDAR) | NP_071731.1:p.Phe398= | |
| XM_006712204.1:c.1290T>C (EDAR) | XP_006712267.1:p.Phe430= | |
| XM_011510502.1:c.1341T>C (EDAR) | XP_011508804.1:p.Phe447= | |
| XM_011510503.1:c.1245T>C (EDAR) | XP_011508805.1:p.Phe415= | |
| XM_011510504.1:c.621T>C (EDAR) | XP_011508806.1:p.Phe207= | |
| XM_011510502.2:c.1434T>C (EDAR) | XP_011508804.2:p.Phe478= | |
| XM_011510503.2:c.1338T>C (EDAR) | XP_011508805.2:p.Phe446= | |
| XM_017004623.2:c.8370+124014A>G (RANBP2) | XP_016860112.1:n.8370+124014A>G | |
| NM_022336.4:c.1194T>C (EDAR) MANE Select | NP_071731.1:p.Phe398= |