Linked Data
ClinVar Variation Id:
2131403
ClinVar RCV Id:
RCV003048185
MyVariant Identifiers:
chr19:g.7504877C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7439991C>A , CM000681.2:g.7439991C>A | GRCh38 |
| NC_000019.9:g.7504877C>A , CM000681.1:g.7504877C>A | GRCh37 |
| NC_000019.8:g.7410877C>A | NCBI36 |
| NG_047135.1:g.96081C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000319670.14:c.-71-353C>A | ENSP00000319200.8:n.-71-353C>A | |
| ENST00000359920.11:c.-112C>A | ENSP00000352995.5:n.-112C>A | |
| ENST00000594665.2:c.-71-353C>A | ENSP00000470729.2:n.-71-353C>A | |
| ENST00000617428.4:c.-226-198C>A | ENSP00000482647.4:n.-226-198C>A | |
| ENST00000668164.2:c.968-353C>A MANE Select | ENSP00000499655.2:n.968-353C>A | |
| ENST00000319670.13:c.-71-353C>A | ENSP00000319200.7:n.-71-353C>A | |
| ENST00000359920.10:c.51C>A | ENSP00000352995.4:p.Ala17= | |
| ENST00000599752.5:c.-226-198C>A | ENSP00000471597.1:n.-226-198C>A | |
| ENST00000617428.2:c.204-353C>A | ||
| NM_001130955.1:c.51C>A | NP_001124427.1:p.Ala17= | |
| NM_015318.3:c.-71-353C>A | NP_056133.2:n.-71-353C>A | |
| XM_005272464.3:c.1163-353C>A | XP_005272521.1:n.1163-353C>A | |
| XM_006722705.2:c.968-353C>A | XP_006722768.1:n.968-353C>A | |
| XM_006722706.2:c.968-353C>A | XP_006722769.1:n.968-353C>A | |
| XM_006722708.2:c.-226-198C>A | XP_006722771.1:n.-226-198C>A | |
| XM_006722709.2:c.-71-353C>A | XP_006722772.1:n.-71-353C>A | |
| XM_011527835.1:c.1163-353C>A | XP_011526137.1:n.1163-353C>A | |
| XM_011527836.1:c.1163-353C>A | XP_011526138.1:n.1163-353C>A | |
| XM_011527837.1:c.1163-353C>A | XP_011526139.1:n.1163-353C>A | |
| XM_011527838.1:c.968-353C>A | XP_011526140.1:n.968-353C>A | |
| XM_011527839.1:c.920-353C>A | XP_011526141.1:n.920-353C>A | |
| XM_011527840.1:c.-71-353C>A | XP_011526142.1:n.-71-353C>A | |
| XM_011527841.1:c.1163-353C>A | XP_011526143.1:n.1163-353C>A | |
| XM_005272464.4:c.1163-353C>A | XP_005272521.1:n.1163-353C>A | |
| XM_006722705.3:c.968-353C>A | XP_006722768.1:n.968-353C>A | |
| XM_006722706.3:c.968-353C>A | XP_006722769.1:n.968-353C>A | |
| XM_011527835.2:c.1163-353C>A | XP_011526137.1:n.1163-353C>A | |
| XM_011527836.2:c.1163-353C>A | XP_011526138.1:n.1163-353C>A | |
| XM_011527837.2:c.1163-353C>A | XP_011526139.1:n.1163-353C>A | |
| XM_011527838.3:c.968-353C>A | XP_011526140.1:n.968-353C>A | |
| XM_011527839.2:c.920-353C>A | XP_011526141.1:n.920-353C>A | |
| XM_011527840.2:c.-71-353C>A | XP_011526142.1:n.-71-353C>A | |
| XM_011527841.2:c.1163-353C>A | XP_011526143.1:n.1163-353C>A | |
| NM_001130955.2:c.-112C>A | NP_001124427.2:n.-112C>A | |
| NM_001367823.1:c.968-353C>A MANE Select | NP_001354752.1:n.968-353C>A | |
| NM_001367824.1:c.-226-198C>A | NP_001354753.1:n.-226-198C>A | |
| NM_015318.4:c.-71-353C>A | NP_056133.2:n.-71-353C>A |