Linked Data
ClinVar Variation Id:
3007103
ClinVar RCV Id:
RCV003868742
dbSNP Id:
rs761944980
ExAC:
12:52912911 C / T
gnomAD v2:
12-52912911-C-T
gnomAD v4:
12-52519127-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52519127C>T , CM000674.2:g.52519127C>T | GRCh38 |
| NC_000012.11:g.52912911C>T , CM000674.1:g.52912911C>T | GRCh37 |
| NC_000012.10:g.51199178C>T | NCBI36 |
| NG_008297.1:g.6333G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252242.9:c.589G>A MANE Select | ENSP00000252242.4:p.Asp197Asn | |
| ENST00000252242.8:c.589G>A | ENSP00000252242.4:p.Asp197Asn | |
| ENST00000549420.1:c.259G>A | ENSP00000447209.1:p.Asp87Asn | |
| ENST00000551013.1:n.117G>A | ||
| ENST00000552629.5:n.687G>A | ||
| NM_000424.3:c.589G>A | NP_000415.2:p.Asp197Asn | |
| NM_000424.4:c.589G>A MANE Select | NP_000415.2:p.Asp197Asn |