Linked Data
ClinVar Variation Id:
865556
ClinVar RCV Id:
RCV001072996
dbSNP Id:
rs2052173415
gnomAD v4:
17-43067649-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43067649T>C , CM000679.2:g.43067649T>C | GRCh38 |
| NC_000017.10:g.41219666T>C , CM000679.1:g.41219666T>C | GRCh37 |
| NC_000017.9:g.38473192T>C | NCBI36 |
| NG_005905.2:g.150335A>G , LRG_292:g.150335A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461574.2:c.5030A>G | ENSP00000417241.2:p.Asn1677Ser | |
| ENST00000470026.6:c.5033A>G | ENSP00000419274.2:p.Asn1678Ser | |
| ENST00000473961.6:c.4907A>G | ENSP00000420201.2:p.Asn1636Ser | |
| ENST00000476777.6:c.5027A>G | ENSP00000417554.2:p.Asn1676Ser | |
| ENST00000477152.6:c.4955A>G | ENSP00000419988.2:p.Asn1652Ser | |
| ENST00000478531.6:c.1721A>G | ENSP00000420412.2:p.Asn574Ser | |
| ENST00000489037.2:c.4955A>G | ENSP00000420781.2:p.Asn1652Ser | |
| ENST00000493919.6:c.1583A>G | ENSP00000418819.2:p.Asn528Ser | |
| ENST00000494123.6:c.5033A>G | ENSP00000419103.2:p.Asn1678Ser | |
| ENST00000497488.2:c.4145A>G | ENSP00000418986.2:p.Asn1382Ser | |
| ENST00000618469.2:c.5033A>G | ENSP00000478114.2:p.Asn1678Ser | |
| ENST00000634433.2:c.4910A>G | ENSP00000489431.2:p.Asn1637Ser | |
| ENST00000644379.2:c.5099A>G | ENSP00000496570.2:p.Asn1700Ser | |
| ENST00000644555.2:c.1583A>G | ENSP00000494614.2:p.Asn528Ser | |
| ENST00000652672.2:c.4892A>G | ENSP00000498906.2:p.Asn1631Ser | |
| ENST00000484087.6:c.1595A>G | ENSP00000419481.2:p.Asn532Ser | |
| ENST00000357654.9:c.5033A>G MANE Select | ENSP00000350283.3:p.Asn1678Ser | |
| ENST00000471181.7:c.5096A>G | ENSP00000418960.2:p.Asn1699Ser | |
| ENST00000644379.1:c.1420A>G | ||
| ENST00000352993.7:c.1607A>G | ENSP00000312236.5:p.Asn536Ser | |
| ENST00000357654.7:c.5033A>G | ENSP00000350283.3:p.Asn1678Ser | |
| ENST00000461221.5:c.*4816A>G | ENSP00000418548.1:n.*4816A>G | |
| ENST00000468300.5:c.1721A>G | ENSP00000417148.1:p.Asn574Ser | |
| ENST00000471181.6:c.5096A>G | ENSP00000418960.2:p.Asn1699Ser | |
| ENST00000472490.1:n.186A>G | ||
| ENST00000478531.5:c.1721A>G | ENSP00000420412.1:p.Asn574Ser | |
| ENST00000484087.5:c.1346A>G | ENSP00000419481.1:p.Asn449Ser | |
| ENST00000491747.6:c.1721A>G | ENSP00000420705.2:p.Asn574Ser | |
| ENST00000493795.5:c.4892A>G | ENSP00000418775.1:p.Asn1631Ser | |
| ENST00000493919.5:c.1583A>G | ENSP00000418819.1:p.Asn528Ser | |
| ENST00000586385.5:c.5-3698A>G | ENSP00000465818.1:n.5-3698A>G | |
| ENST00000591534.5:c.506A>G | ENSP00000467329.1:p.Asn169Ser | |
| ENST00000591849.5:c.-98-17459A>G | ENSP00000465347.1:n.-98-17459A>G | |
| NM_007294.3:c.5033A>G , LRG_292t1:c.5033A>G | NP_009225.1:p.Asn1678Ser | |
| NM_007297.3:c.4892A>G | NP_009228.2:p.Asn1631Ser | |
| NM_007298.3:c.1721A>G | NP_009229.2:p.Asn574Ser | |
| NM_007299.3:c.1721A>G | NP_009230.2:p.Asn574Ser | |
| NM_007300.3:c.5096A>G | NP_009231.2:p.Asn1699Ser | |
| NR_027676.1:n.5169A>G | ||
| NM_007294.4:c.5033A>G MANE Select | NP_009225.1:p.Asn1678Ser | |
| NM_007297.4:c.4892A>G | NP_009228.2:p.Asn1631Ser | |
| NM_007299.4:c.1721A>G | NP_009230.2:p.Asn574Ser | |
| NM_007300.4:c.5096A>G | NP_009231.2:p.Asn1699Ser | |
| NR_027676.2:n.5210A>G |