Linked Data
ClinVar Variation Id:
166729
dbSNP Id:
rs144855583
ExAC:
4:123664553 C / T
gnomAD v2:
4-123664553-C-T
gnomAD v3:
4-122743398-C-T
gnomAD v4:
4-122743398-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.122743398C>T , CM000666.2:g.122743398C>T | GRCh38 |
| NC_000004.11:g.123664553C>T , CM000666.1:g.123664553C>T | GRCh37 |
| NC_000004.10:g.123884003C>T | NCBI36 |
| NG_021203.1:g.15697C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000314218.8:c.1506C>T MANE Select | ENSP00000319062.3:p.Ala502= | |
| ENST00000314218.7:c.1506C>T | ENSP00000319062.3:p.Ala502= | |
| ENST00000542236.5:c.1506C>T | ENSP00000438273.1:p.Ala502= | |
| NM_001178007.1:c.1506C>T | NP_001171478.1:p.Ala502= | |
| NM_152618.2:c.1506C>T | NP_689831.2:p.Ala502= | |
| XM_011531680.1:c.1506C>T | XP_011529982.1:p.Ala502= | |
| XM_011531680.2:c.1506C>T | XP_011529982.1:p.Ala502= | |
| XM_017007831.1:c.1506C>T | XP_016863320.1:p.Ala502= | |
| NM_152618.3:c.1506C>T MANE Select | NP_689831.2:p.Ala502= | |
| NM_001178007.2:c.1506C>T | NP_001171478.1:p.Ala502= |