Linked Data
ClinVar Variation Id:
874160
ClinVar RCV Id:
RCV001096865
dbSNP Id:
rs747330693
ExAC:
1:197111525 A / G
gnomAD v2:
1-197111525-A-G
gnomAD v3:
1-197142395-A-G
gnomAD v4:
1-197142395-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.197142395A>G , CM000663.2:g.197142395A>G | GRCh38 |
| NC_000001.10:g.197111525A>G , CM000663.1:g.197111525A>G | GRCh37 |
| NC_000001.9:g.195378148A>G | NCBI36 |
| NG_015867.1:g.9300T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367409.9:c.1857T>C MANE Select | ENSP00000356379.4:p.Asn619= | |
| ENST00000679766.1:n.2074T>C | ||
| ENST00000680265.1:c.1857T>C | ENSP00000505384.1:p.Asn619= | |
| ENST00000680710.1:c.1857T>C | ENSP00000506676.1:p.Asn619= | |
| ENST00000681879.1:c.1857T>C | ENSP00000505363.1:p.Asn619= | |
| ENST00000294732.11:c.1857T>C | ENSP00000294732.7:p.Asn619= | |
| ENST00000367409.8:c.1857T>C | ENSP00000356379.4:p.Asn619= | |
| ENST00000612785.1:c.561+1296T>C | ENSP00000479244.1:n.561+1296T>C | |
| NM_001206846.1:c.1857T>C | NP_001193775.1:p.Asn619= | |
| NM_018136.4:c.1857T>C | NP_060606.3:p.Asn619= | |
| NM_018136.5:c.1857T>C MANE Select | NP_060606.3:p.Asn619= | |
| NM_001206846.2:c.1857T>C | NP_001193775.1:p.Asn619= |