Linked Data
ClinVar Variation Id:
408539
dbSNP Id:
rs754778750
ExAC:
2:47693881 T / C
gnomAD v2:
2-47693881-T-C
gnomAD v4:
2-47466742-T-C
PubMed:
PMID:25980754
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47466742T>C , CM000664.2:g.47466742T>C | GRCh38 |
| NC_000002.11:g.47693881T>C , CM000664.1:g.47693881T>C | GRCh37 |
| NC_000002.10:g.47547385T>C | NCBI36 |
| NG_007110.2:g.68619T>C , LRG_218:g.68619T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644900.2:c.1595T>C | ENSP00000495641.2:p.Val532Ala | |
| ENST00000233146.7:c.1595T>C MANE Select | ENSP00000233146.2:p.Val532Ala | |
| ENST00000543555.6:c.1397T>C | ENSP00000442697.1:p.Val466Ala | |
| ENST00000644092.1:c.1595T>C | ENSP00000496351.1:p.Val532Ala | |
| ENST00000645339.1:c.1595T>C | ENSP00000496441.1:p.Val532Ala | |
| ENST00000645506.1:c.1595T>C | ENSP00000495455.1:p.Val532Ala | |
| ENST00000646415.1:c.1595T>C | ENSP00000495543.1:p.Val532Ala | |
| ENST00000233146.6:c.1595T>C | ENSP00000233146.2:p.Val532Ala | |
| ENST00000406134.5:c.1595T>C | ENSP00000384199.1:p.Val532Ala | |
| ENST00000543555.5:c.1397T>C | ENSP00000442697.1:p.Val466Ala | |
| ENST00000610696.4:c.1593T>C | ENSP00000483159.1:p.Ser531= | |
| ENST00000613514.4:c.*135T>C | ENSP00000484137.1:n.*135T>C | |
| ENST00000617333.3:c.*361T>C | ENSP00000482468.1:n.*361T>C | |
| ENST00000617938.4:c.*567T>C | ENSP00000481158.1:n.*567T>C | |
| ENST00000621359.2:c.1595T>C | ENSP00000481416.1:p.Val532Ala | |
| NM_000251.2:c.1595T>C , LRG_218t1:c.1595T>C | NP_000242.1:p.Val532Ala | |
| NM_001258281.1:c.1397T>C | NP_001245210.1:p.Val466Ala | |
| XM_005264332.2:c.1595T>C | XP_005264389.2:p.Val532Ala | |
| XM_011532867.1:c.1595T>C | XP_011531169.1:p.Val532Ala | |
| XR_939685.1:n.1667T>C | ||
| XM_005264332.4:c.1595T>C | XP_005264389.2:p.Val532Ala | |
| XM_011532867.2:c.1595T>C | XP_011531169.1:p.Val532Ala | |
| XR_001738747.2:n.1657T>C | ||
| XR_939685.2:n.1657T>C | ||
| NM_000251.3:c.1595T>C MANE Select | NP_000242.1:p.Val532Ala |