Linked Data
ClinVar Variation Id:
755219
dbSNP Id:
rs1575932637
gnomAD v4:
3-10149929-A-C
MyVariant Identifiers:
chr3:g.10191613A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10149929A>C , CM000665.2:g.10149929A>C | GRCh38 |
| NC_000003.11:g.10191613A>C , CM000665.1:g.10191613A>C | GRCh37 |
| NC_000003.10:g.10166613A>C | NCBI36 |
| NG_008212.3:g.13295A>C , LRG_322:g.13295A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696142.1:c.*283A>C | ENSP00000512434.1:n.*283A>C | |
| ENST00000696143.1:c.742A>C | ENSP00000512435.1:n.742A>C | |
| ENST00000696153.1:c.717A>C | ENSP00000512444.1:p.Thr239= | |
| ENST00000256474.3:c.606A>C MANE Select | ENSP00000256474.3:p.Thr202= | |
| ENST00000256474.2:c.606A>C | ENSP00000256474.2:p.Thr202= | |
| ENST00000345392.2:c.483A>C | ENSP00000344757.2:p.Thr161= | |
| ENST00000477538.1:n.742A>C | ||
| NM_000551.3:c.606A>C , LRG_322t1:c.606A>C | NP_000542.1:p.Thr202= | |
| NM_198156.2:c.483A>C | NP_937799.1:p.Thr161= | |
| NM_001354723.1:c.*160A>C | NP_001341652.1:n.*160A>C | |
| NM_000551.4:c.606A>C MANE Select | NP_000542.1:p.Thr202= | |
| NM_001354723.2:c.*160A>C | NP_001341652.1:n.*160A>C | |
| NM_198156.3:c.483A>C | NP_937799.1:p.Thr161= |