Linked Data
ClinVar Variation Id:
68788
ClinVar RCV Id:
RCV000059736
RCV000122056
RCV000488661
RCV000561032
RCV000662613
RCV001293427
RCV002311543
RCV003315582
dbSNP Id:
rs281875323
ExAC:
18:48573454 A / G
gnomAD v2:
18-48573454-A-G
gnomAD v4:
18-51047084-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.51047084A>G , CM000680.2:g.51047084A>G | GRCh38 |
| NC_000018.9:g.48573454A>G , CM000680.1:g.48573454A>G | GRCh37 |
| NC_000018.8:g.46827452A>G | NCBI36 |
| NG_013013.2:g.84045A>G , LRG_318:g.84045A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000588860.6:c.38A>G | ENSP00000465878.2:p.Asn13Ser | |
| ENST00000589076.6:c.38A>G | ENSP00000466934.2:p.Asn13Ser | |
| ENST00000589941.2:c.38A>G | ENSP00000465874.2:p.Asn13Ser | |
| ENST00000590061.2:c.38A>G | ENSP00000464772.2:p.Asn13Ser | |
| ENST00000593223.2:c.38A>G | ENSP00000466118.2:p.Asn13Ser | |
| ENST00000611848.2:c.38A>G | ENSP00000478613.2:p.Asn13Ser | |
| ENST00000342988.8:c.38A>G MANE Select | ENSP00000341551.3:p.Asn13Ser | |
| ENST00000342988.7:c.38A>G | ENSP00000341551.3:p.Asn13Ser | |
| ENST00000398417.6:c.38A>G | ENSP00000381452.1:p.Asn13Ser | |
| ENST00000588256.1:n.499A>G | ||
| ENST00000588745.5:c.38A>G | ENSP00000464901.1:p.Asn13Ser | |
| ENST00000588860.5:c.38A>G | ENSP00000465878.1:p.Asn13Ser | |
| ENST00000589076.5:c.38A>G | ENSP00000466934.1:p.Asn13Ser | |
| ENST00000589941.1:c.38A>G | ENSP00000465874.1:p.Asn13Ser | |
| ENST00000590061.1:c.38A>G | ENSP00000464772.1:p.Asn13Ser | |
| ENST00000590722.2:c.*61A>G | ENSP00000465737.1:n.*61A>G | |
| ENST00000591914.5:c.38A>G | ENSP00000466941.1:p.Asn13Ser | |
| ENST00000592186.5:c.38A>G | ENSP00000468611.1:p.Asn13Ser | |
| ENST00000592911.5:n.28-1602A>G | ||
| NM_005359.5:c.38A>G , LRG_318t1:c.38A>G | NP_005350.1:p.Asn13Ser | |
| NM_005359.6:c.38A>G MANE Select | NP_005350.1:p.Asn13Ser |