Linked Data
ClinVar Variation Id:
326370
ClinVar RCV Id:
RCV000398657
dbSNP Id:
rs749440073
gnomAD v2:
18-28646823-T-C
gnomAD v3:
18-31066857-T-C
gnomAD v4:
18-31066857-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31066857T>C , CM000680.2:g.31066857T>C | GRCh38 |
| NC_000018.9:g.28646823T>C , CM000680.1:g.28646823T>C | GRCh37 |
| NC_000018.8:g.26900821T>C | NCBI36 |
| NG_008208.2:g.40569A>G , LRG_400:g.40569A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682357.1:c.*1158A>G | ENSP00000507826.1:n.*1158A>G | |
| ENST00000251081.8:c.*1366A>G | ENSP00000251081.6:n.*1366A>G | |
| ENST00000280904.11:c.*1158A>G MANE Select | ENSP00000280904.6:n.*1158A>G | |
| ENST00000648081.1:c.*1158A>G | ENSP00000497441.1:n.*1158A>G | |
| ENST00000251081.6:c.*1366A>G | ENSP00000251081.6:n.*1366A>G | |
| ENST00000280904.10:c.*1158A>G | ENSP00000280904.6:n.*1158A>G | |
| NM_004949.4:c.*1366A>G | NP_004940.1:n.*1366A>G | |
| NM_024422.4:c.*1158A>G | NP_077740.1:n.*1158A>G | |
| XM_005258206.3:c.*1158A>G | XP_005258263.1:n.*1158A>G | |
| XM_005258206.4:c.*1158A>G | XP_005258263.1:n.*1158A>G | |
| NM_004949.5:c.*1366A>G | NP_004940.1:n.*1366A>G | |
| NM_024422.6:c.*1158A>G MANE Select | NP_077740.1:n.*1158A>G |