Linked Data
ClinVar Variation Id:
135245
ClinVar RCV Id:
RCV000122059
RCV000132146
RCV000411125
RCV000657009
RCV000770697
RCV001358781
RCV002311007
RCV003315779
dbSNP Id:
rs377119288
ExAC:
18:48586278 A / G
gnomAD v2:
18-48586278-A-G
gnomAD v3:
18-51059908-A-G
gnomAD v4:
18-51059908-A-G
PubMed:
PMID:24728327
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.51059908A>G , CM000680.2:g.51059908A>G | GRCh38 |
| NC_000018.9:g.48586278A>G , CM000680.1:g.48586278A>G | GRCh37 |
| NC_000018.8:g.46840276A>G | NCBI36 |
| NG_013013.2:g.96869A>G , LRG_318:g.96869A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000588860.6:c.947A>G | ENSP00000465878.2:p.Asn316Ser | |
| ENST00000589076.6:c.947A>G | ENSP00000466934.2:p.Asn316Ser | |
| ENST00000589941.2:c.947A>G | ENSP00000465874.2:p.Asn316Ser | |
| ENST00000590061.2:c.947A>G | ENSP00000464772.2:p.Asn316Ser | |
| ENST00000593223.2:c.947A>G | ENSP00000466118.2:p.Asn316Ser | |
| ENST00000611848.2:c.947A>G | ENSP00000478613.2:p.Asn316Ser | |
| ENST00000684953.1:n.2319A>G | ||
| ENST00000685090.1:n.1398A>G | ||
| ENST00000685232.1:n.1055A>G | ||
| ENST00000688307.1:n.198A>G | ||
| ENST00000688574.1:n.1055A>G | ||
| ENST00000688903.1:n.1161A>G | ||
| ENST00000690892.1:n.1055A>G | ||
| ENST00000342988.8:c.947A>G MANE Select | ENSP00000341551.3:p.Asn316Ser | |
| ENST00000342988.7:c.947A>G | ENSP00000341551.3:p.Asn316Ser | |
| ENST00000398417.6:c.947A>G | ENSP00000381452.1:p.Asn316Ser | |
| ENST00000588745.5:c.667+4915A>G | ENSP00000464901.1:n.667+4915A>G | |
| ENST00000591126.5:n.2948A>G | ||
| ENST00000592186.5:c.947A>G | ENSP00000468611.1:p.Asn316Ser | |
| ENST00000611848.1:c.147A>G | ||
| NM_005359.5:c.947A>G , LRG_318t1:c.947A>G | NP_005350.1:p.Asn316Ser | |
| NM_005359.6:c.947A>G MANE Select | NP_005350.1:p.Asn316Ser |