Linked Data
ClinVar Variation Id:
746138
ClinVar RCV Id:
RCV001477327
dbSNP Id:
rs1252473811
gnomAD v2:
3-10191478-T-C
gnomAD v3:
3-10149794-T-C
gnomAD v4:
3-10149794-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10149794T>C , CM000665.2:g.10149794T>C | GRCh38 |
| NC_000003.11:g.10191478T>C , CM000665.1:g.10191478T>C | GRCh37 |
| NC_000003.10:g.10166478T>C | NCBI36 |
| NG_008212.3:g.13160T>C , LRG_322:g.13160T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000696142.1:c.*148T>C | ENSP00000512434.1:n.*148T>C | |
| ENST00000696143.1:c.607T>C | ENSP00000512435.1:n.607T>C | |
| ENST00000696153.1:c.582T>C | ENSP00000512444.1:p.Thr194= | |
| ENST00000256474.3:c.471T>C MANE Select | ENSP00000256474.3:p.Thr157= | |
| ENST00000256474.2:c.471T>C | ENSP00000256474.2:p.Thr157= | |
| ENST00000345392.2:c.348T>C | ENSP00000344757.2:p.Thr116= | |
| ENST00000477538.1:n.607T>C | ||
| NM_000551.3:c.471T>C , LRG_322t1:c.471T>C | NP_000542.1:p.Thr157= | |
| NM_198156.2:c.348T>C | NP_937799.1:p.Thr116= | |
| NM_001354723.1:c.*25T>C | NP_001341652.1:n.*25T>C | |
| NM_000551.4:c.471T>C MANE Select | NP_000542.1:p.Thr157= | |
| NM_001354723.2:c.*25T>C | NP_001341652.1:n.*25T>C | |
| NM_198156.3:c.348T>C | NP_937799.1:p.Thr116= |