Linked Data
ClinVar Variation Id:
466111
dbSNP Id:
rs1263094349
gnomAD v2:
9-135772094-T-C
gnomAD v3:
9-132896707-T-C
gnomAD v4:
9-132896707-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.132896707T>C , CM000671.2:g.132896707T>C | GRCh38 |
| NC_000009.11:g.135772094T>C , CM000671.1:g.135772094T>C | GRCh37 |
| NC_000009.10:g.134761915T>C | NCBI36 |
| NG_012386.1:g.52927A>G , LRG_486:g.52927A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000475903.7:c.3020A>G | ENSP00000496126.2:p.Asn1007Ser | |
| ENST00000490179.4:c.3023A>G | ENSP00000495533.2:p.Asn1008Ser | |
| ENST00000642261.2:c.*879A>G | ENSP00000494743.2:n.*879A>G | |
| ENST00000643275.2:c.*963A>G | ENSP00000495598.2:n.*963A>G | |
| ENST00000643362.2:c.2636A>G | ENSP00000496398.2:p.Asn879Ser | |
| ENST00000643625.2:c.*765A>G | ENSP00000495546.2:n.*765A>G | |
| ENST00000643691.2:c.2660A>G | ENSP00000494916.2:p.Asn887Ser | |
| ENST00000644184.2:c.2981A>G | ENSP00000495428.2:p.Asn994Ser | |
| ENST00000645129.2:c.2867A>G | ENSP00000493639.2:p.Asn956Ser | |
| ENST00000646440.2:c.3023A>G | ENSP00000495830.2:p.Asn1008Ser | |
| ENST00000298552.9:c.3023A>G MANE Select | ENSP00000298552.3:p.Asn1008Ser | |
| ENST00000642261.1:c.1160A>G | ||
| ENST00000642617.1:c.3020A>G | ENSP00000493773.1:p.Asn1007Ser | |
| ENST00000642627.1:c.3005A>G | ENSP00000496772.1:p.Asn1002Ser | |
| ENST00000642811.1:c.*2793A>G | ENSP00000495554.1:n.*2793A>G | |
| ENST00000643072.1:c.2870A>G | ENSP00000496691.1:p.Asn957Ser | |
| ENST00000643275.1:c.1497A>G | ENSP00000495598.1:n.1497A>G | |
| ENST00000643583.1:c.3008A>G | ENSP00000494685.1:p.Asn1003Ser | |
| ENST00000643625.1:c.900A>G | ENSP00000495546.1:n.900A>G | |
| ENST00000643875.1:c.3023A>G | ENSP00000495158.1:p.Asn1008Ser | |
| ENST00000644097.1:c.3020A>G | ENSP00000494682.1:p.Asn1007Ser | |
| ENST00000644184.1:c.1718A>G | ENSP00000495428.1:p.Asn573Ser | |
| ENST00000644255.1:c.*2790A>G | ENSP00000493608.1:n.*2790A>G | |
| ENST00000644319.1:n.3398A>G | ||
| ENST00000644786.1:n.682A>G | ||
| ENST00000644882.1:n.1931A>G | ||
| ENST00000645901.1:n.3874A>G | ||
| ENST00000646391.1:c.*2793A>G | ENSP00000494104.1:n.*2793A>G | |
| ENST00000646625.1:c.3023A>G | ENSP00000496263.1:p.Asn1008Ser | |
| ENST00000647262.1:n.1988A>G | ||
| ENST00000647279.1:c.*2262A>G | ENSP00000494502.1:n.*2262A>G | |
| ENST00000647534.1:n.2087A>G | ||
| ENST00000298552.7:c.3023A>G | ENSP00000298552.3:p.Asn1008Ser | |
| ENST00000440111.6:c.3023A>G | ENSP00000394524.2:p.Asn1008Ser | |
| ENST00000545250.5:c.2870A>G | ENSP00000444017.1:p.Asn957Ser | |
| NM_000368.4:c.3023A>G , LRG_486t1:c.3023A>G | NP_000359.1:p.Asn1008Ser | |
| NM_001162426.1:c.3020A>G | NP_001155898.1:p.Asn1007Ser | |
| NM_001162427.1:c.2870A>G | NP_001155899.1:p.Asn957Ser | |
| XM_005272211.1:c.3023A>G | XP_005272268.1:p.Asn1008Ser | |
| XM_006717271.1:c.3023A>G | XP_006717334.1:p.Asn1008Ser | |
| XM_011518979.1:c.3023A>G | XP_011517281.1:p.Asn1008Ser | |
| NM_001362177.1:c.2660A>G | NP_001349106.1:p.Asn887Ser | |
| XM_011518979.2:c.3023A>G | XP_011517281.1:p.Asn1008Ser | |
| XM_017015096.1:c.3023A>G | XP_016870585.1:p.Asn1008Ser | |
| XM_017015097.1:c.3023A>G | XP_016870586.1:p.Asn1008Ser | |
| XM_017015098.1:c.3020A>G | XP_016870587.1:p.Asn1007Ser | |
| XM_017015100.1:c.2660A>G | XP_016870589.1:p.Asn887Ser | |
| XM_017015101.1:c.2657A>G | XP_016870590.1:p.Asn886Ser | |
| NM_000368.5:c.3023A>G MANE Select | NP_000359.1:p.Asn1008Ser | |
| NM_001162426.2:c.3020A>G | NP_001155898.1:p.Asn1007Ser | |
| NM_001162427.2:c.2870A>G | NP_001155899.1:p.Asn957Ser | |
| NM_001362177.2:c.2660A>G | NP_001349106.1:p.Asn887Ser |