Linked Data
ClinVar Variation Id:
262725
dbSNP Id:
rs855791
ExAC:
22:37462936 A / G
gnomAD v2:
22-37462936-A-G
gnomAD v3:
22-37066896-A-G
gnomAD v4:
22-37066896-A-G
PubMed:
PMID:19820699
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.37066896A>G , CM000684.2:g.37066896A>G | GRCh38 |
| NC_000022.10:g.37462936A>G , CM000684.1:g.37462936A>G | GRCh37 |
| NC_000022.9:g.35792882A>G | NCBI36 |
| NG_012856.2:g.47668T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000346753.9:c.2180T>C | ENSP00000334962.6:p.Val727Ala | |
| ENST00000406725.6:c.2180T>C | ENSP00000385453.1:p.Val727Ala | |
| ENST00000406856.7:c.2246T>C | ENSP00000384964.1:p.Val749Ala | |
| ENST00000676104.1:c.2180T>C MANE Select | ENSP00000501573.1:p.Val727Ala | |
| ENST00000346753.7:c.2207T>C | ENSP00000334962.5:p.Val736Ala | |
| ENST00000381792.6:c.2246T>C | ENSP00000371211.2:p.Val749Ala | |
| ENST00000406725.5:c.2180T>C | ENSP00000385453.1:p.Val727Ala | |
| ENST00000406856.5:c.2246T>C | ENSP00000384964.1:p.Val749Ala | |
| NM_001289000.1:c.2246T>C | NP_001275929.1:p.Val749Ala | |
| NM_001289001.1:c.2180T>C | NP_001275930.1:p.Val727Ala | |
| NM_153609.3:c.2207T>C | NP_705837.1:p.Val736Ala | |
| XM_006724162.1:c.2180T>C | XP_006724225.1:p.Val727Ala | |
| XM_006724163.2:c.2180T>C | XP_006724226.1:p.Val727Ala | |
| XM_011529987.1:c.2246T>C | XP_011528289.1:p.Val749Ala | |
| XM_011529988.1:c.2246T>C | XP_011528290.1:p.Val749Ala | |
| XM_011529989.1:c.1814T>C | XP_011528291.1:p.Val605Ala | |
| XM_011529989.2:c.1814T>C | XP_011528291.1:p.Val605Ala | |
| XM_024452167.1:c.2246T>C | XP_024307935.1:p.Val749Ala | |
| XM_024452168.1:c.2246T>C | XP_024307936.1:p.Val749Ala | |
| XM_024452169.1:c.2246T>C | XP_024307937.1:p.Val749Ala | |
| XM_024452170.1:c.2180T>C | XP_024307938.1:p.Val727Ala | |
| XM_024452171.1:c.2180T>C | XP_024307939.1:p.Val727Ala | |
| NM_001289000.2:c.2246T>C | NP_001275929.1:p.Val749Ala | |
| NM_001289001.2:c.2180T>C | NP_001275930.1:p.Val727Ala | |
| NM_001374504.1:c.2180T>C MANE Select | NP_001361433.1:p.Val727Ala | |
| NM_153609.4:c.2180T>C | NP_705837.2:p.Val727Ala |