Linked Data
dbSNP Id:
rs368571532
ExAC:
2:109513406 G / A
gnomAD v2:
2-109513406-G-A
gnomAD v3:
2-108896950-G-A
gnomAD v4:
2-108896950-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.108896950G>A , CM000664.2:g.108896950G>A | GRCh38 |
| NC_000002.11:g.109513406G>A , CM000664.1:g.109513406G>A | GRCh37 |
| NC_000002.10:g.108879838G>A | NCBI36 |
| NG_008257.1:g.97423C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258443.7:c.1304C>T (EDAR) MANE Select | ENSP00000258443.2:p.Ala435Val | |
| ENST00000258443.6:c.1304C>T (EDAR) | ENSP00000258443.2:p.Ala435Val | |
| ENST00000376651.1:c.1400C>T (EDAR) | ENSP00000365839.1:p.Ala467Val | |
| ENST00000409271.5:c.1400C>T (EDAR) | ENSP00000386371.1:p.Ala467Val | |
| NM_022336.3:c.1304C>T (EDAR) | NP_071731.1:p.Ala435Val | |
| XM_006712204.1:c.1400C>T (EDAR) | XP_006712267.1:p.Ala467Val | |
| XM_011510502.1:c.1451C>T (EDAR) | XP_011508804.1:p.Ala484Val | |
| XM_011510503.1:c.1355C>T (EDAR) | XP_011508805.1:p.Ala452Val | |
| XM_011510504.1:c.731C>T (EDAR) | XP_011508806.1:p.Ala244Val | |
| XM_011510502.2:c.1544C>T (EDAR) | XP_011508804.2:p.Ala515Val | |
| XM_011510503.2:c.1448C>T (EDAR) | XP_011508805.2:p.Ala483Val | |
| XM_017004623.2:c.8370+123904G>A (RANBP2) | XP_016860112.1:n.8370+123904G>A | |
| NM_022336.4:c.1304C>T (EDAR) MANE Select | NP_071731.1:p.Ala435Val |