Linked Data
ClinVar Variation Id:
1080717
ClinVar RCV Id:
RCV001396438
dbSNP Id:
rs774624157
ExAC:
4:5809973 C / T
gnomAD v2:
4-5809973-C-T
gnomAD v4:
4-5808246-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.5808246C>T , CM000666.2:g.5808246C>T | GRCh38 |
| NC_000004.11:g.5809973C>T , CM000666.1:g.5809973C>T | GRCh37 |
| NC_000004.10:g.5860874C>T | NCBI36 |
| NG_008843.1:g.102050C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264956.11:c.2607C>T (EVC) MANE Select | ENSP00000264956.6:p.His869= | |
| ENST00000264956.10:c.2607C>T (EVC) | ENSP00000264956.6:p.His869= | |
| ENST00000506216.5:n.1647+17248G>A (CRMP1) | ||
| NM_001306090.1:c.2607C>T (EVC) | NP_001293019.1:p.His869= | |
| NM_153717.2:c.2607C>T (EVC) | NP_714928.1:p.His869= | |
| XM_006713865.2:c.2607C>T (EVC) | XP_006713928.1:p.His869= | |
| XM_006713866.2:c.2607C>T (EVC) | XP_006713929.1:p.His869= | |
| XR_427473.2:n.2797C>T (EVC) | ||
| XR_427475.2:n.2797C>T (EVC) | ||
| XR_427476.2:n.2797C>T (EVC) | ||
| XR_924920.1:n.2797C>T (EVC) | ||
| XR_924921.1:n.2797C>T (EVC) | ||
| XR_924922.1:n.2797C>T (EVC) | ||
| XR_924923.1:n.2797C>T (EVC) | ||
| XR_924924.1:n.2797C>T (EVC) | ||
| XR_924925.1:n.2797C>T (EVC) | ||
| XR_924926.1:n.2797C>T (EVC) | ||
| XR_924927.1:n.2797C>T (EVC) | ||
| XM_006713865.3:c.2607C>T (EVC) | XP_006713928.1:p.His869= | |
| XM_006713866.3:c.2607C>T (EVC) | XP_006713929.1:p.His869= | |
| XR_001741164.1:n.2787C>T (EVC) | ||
| XR_001741165.1:n.2787C>T (EVC) | ||
| XR_001741166.1:n.2787C>T (EVC) | ||
| XR_001741167.1:n.2787C>T (EVC) | ||
| XR_001741168.1:n.2787C>T (EVC) | ||
| XR_001741169.2:n.2651C>T (EVC) | ||
| XR_001741170.1:n.2872C>T (EVC) | ||
| XR_001741171.1:n.2092C>T (EVC) | ||
| XR_427473.3:n.2787C>T (EVC) | ||
| XR_427475.3:n.2787C>T (EVC) | ||
| XR_427476.3:n.2787C>T (EVC) | ||
| XR_924920.2:n.2787C>T (EVC) | ||
| XR_924921.2:n.2787C>T (EVC) | ||
| XR_924922.2:n.2787C>T (EVC) | ||
| XR_924924.2:n.2787C>T (EVC) | ||
| XR_924925.2:n.2787C>T (EVC) | ||
| XR_924926.2:n.2787C>T (EVC) | ||
| NM_153717.3:c.2607C>T (EVC) MANE Select | NP_714928.1:p.His869= | |
| NM_001306090.2:c.2607C>T (EVC) | NP_001293019.1:p.His869= |