Linked Data
ClinVar Variation Id:
342106
dbSNP Id:
rs138153307
ExAC:
22:50512732 G / A
gnomAD v2:
22-50512732-G-A
gnomAD v3:
22-50074303-G-A
gnomAD v4:
22-50074303-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.50074303G>A , CM000684.2:g.50074303G>A | GRCh38 |
| NC_000022.10:g.50512732G>A , CM000684.1:g.50512732G>A | GRCh37 |
| NC_000022.9:g.48854859G>A | NCBI36 |
| NG_009162.1:g.16627C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311597.10:c.627C>T MANE Select | ENSP00000310375.6:p.Ala209= | |
| ENST00000311597.9:c.627C>T | ENSP00000310375.5:p.Ala209= | |
| ENST00000395876.6:c.627C>T | ENSP00000379216.2:p.Ala209= | |
| ENST00000442311.1:c.537C>T | ENSP00000401385.1:p.Ala179= | |
| ENST00000470008.1:n.107C>T | ||
| NM_015166.3:c.627C>T | NP_055981.1:p.Ala209= | |
| NM_139202.2:c.627C>T | NP_631941.1:p.Ala209= | |
| XM_011530678.1:c.627C>T | XP_011528980.1:p.Ala209= | |
| XR_430476.2:n.1022C>T | ||
| XM_011530678.2:c.627C>T | XP_011528980.1:p.Ala209= | |
| XM_017028671.1:c.627C>T | XP_016884160.1:p.Ala209= | |
| XR_001755180.2:n.1132C>T | ||
| XR_001755181.2:n.900C>T | ||
| NM_001376472.1:c.627C>T | NP_001363401.1:p.Ala209= | |
| NM_001376473.1:c.627C>T | NP_001363402.1:p.Ala209= | |
| NM_001376474.1:c.627C>T | NP_001363403.1:p.Ala209= | |
| NM_001376475.1:c.627C>T | NP_001363404.1:p.Ala209= | |
| NM_001376476.1:c.627C>T | NP_001363405.1:p.Ala209= | |
| NM_001376477.1:c.627C>T | NP_001363406.1:p.Ala209= | |
| NM_001376478.1:c.627C>T | NP_001363407.1:p.Ala209= | |
| NM_001376479.1:c.627C>T | NP_001363408.1:p.Ala209= | |
| NM_001376480.1:c.537C>T | NP_001363409.1:p.Ala179= | |
| NM_001376481.1:c.525C>T | NP_001363410.1:p.Ala175= | |
| NM_001376482.1:c.471C>T | NP_001363411.1:p.Ala157= | |
| NM_001376483.1:c.471C>T | NP_001363412.1:p.Ala157= | |
| NM_001376484.1:c.390C>T | NP_001363413.1:p.Ala130= | |
| NM_015166.4:c.627C>T MANE Select | NP_055981.1:p.Ala209= | |
| NM_139202.3:c.627C>T | NP_631941.1:p.Ala209= | |
| NR_164811.1:n.974C>T | ||
| NR_164812.1:n.758C>T | ||
| NR_164813.1:n.1151C>T |