Linked Data
ClinVar Variation Id:
1433302
ClinVar RCV Id:
RCV001960069
dbSNP Id:
rs1464099781
gnomAD v2:
11-88911379-T-G
gnomAD v4:
11-89178211-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.89178211T>G , CM000673.2:g.89178211T>G | GRCh38 |
| NC_000011.9:g.88911379T>G , CM000673.1:g.88911379T>G | GRCh37 |
| NC_000011.8:g.88551027T>G | NCBI36 |
| NG_008748.1:g.5340T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263321.6:c.258T>G MANE Select | ENSP00000263321.4:p.Asn86Lys | |
| ENST00000263321.5:c.258T>G | ENSP00000263321.4:p.Asn86Lys | |
| ENST00000526139.1:n.319T>G | ||
| NM_000372.4:c.258T>G | NP_000363.1:p.Asn86Lys | |
| XM_011542970.1:c.258T>G | XP_011541272.1:p.Asn86Lys | |
| XM_011542970.2:c.258T>G | XP_011541272.1:p.Asn86Lys | |
| XR_001748321.1:n.2718-64678A>C | ||
| XR_001748322.1:n.2733-64678A>C | ||
| NM_000372.5:c.258T>G MANE Select | NP_000363.1:p.Asn86Lys |