Linked Data
ClinVar Variation Id:
2788598
ClinVar RCV Id:
RCV003674164
gnomAD v4:
12-132673665-A-G
MyVariant Identifiers:
chr12:g.133250251A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.132673665A>G , CM000674.2:g.132673665A>G | GRCh38 |
| NC_000012.11:g.133250251A>G , CM000674.1:g.133250251A>G | GRCh37 |
| NC_000012.10:g.131760324A>G | NCBI36 |
| NG_033840.1:g.18860T>C , LRG_789:g.18860T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000545015.2:n.1296T>C | ||
| ENST00000699982.1:c.1123T>C | ||
| ENST00000699983.1:c.1123T>C | ||
| ENST00000699984.1:c.1123T>C | ||
| ENST00000320574.10:c.1269T>C MANE Select | ENSP00000322570.5:p.Asn423= | |
| ENST00000672742.1:c.*771T>C | ENSP00000500279.1:n.*771T>C | |
| ENST00000320574.9:c.1269T>C | ENSP00000322570.5:p.Asn423= | |
| ENST00000535270.5:c.1188T>C | ENSP00000445753.1:p.Asn396= | |
| ENST00000535934.2:n.1144T>C | ||
| ENST00000537064.5:c.*316T>C | ENSP00000442578.1:n.*316T>C | |
| NM_006231.3:c.1269T>C , LRG_789t1:c.1269T>C | NP_006222.2:p.Asn423= | |
| XM_011534795.1:c.1269T>C | XP_011533097.1:p.Asn423= | |
| XM_011534796.1:c.1140T>C | XP_011533098.1:p.Asn380= | |
| XM_011534797.1:c.348T>C | XP_011533099.1:p.Asn116= | |
| XM_011534799.1:c.1269T>C | XP_011533101.1:p.Asn423= | |
| XM_011534800.1:c.1269T>C | XP_011533102.1:p.Asn423= | |
| XM_011534801.1:c.1269T>C | XP_011533103.1:p.Asn423= | |
| XR_941395.1:n.1478T>C | ||
| XM_011534795.3:c.1269T>C | XP_011533097.1:p.Asn423= | |
| XM_011534797.3:c.348T>C | XP_011533099.1:p.Asn116= | |
| XM_011534799.2:c.1269T>C | XP_011533101.1:p.Asn423= | |
| XR_002957338.1:n.1473T>C | ||
| XR_002957339.1:n.1473T>C | ||
| XR_941395.2:n.1473T>C | ||
| NM_006231.4:c.1269T>C MANE Select | NP_006222.2:p.Asn423= |