Linked Data
ClinVar Variation Id:
2095090
ClinVar RCV Id:
RCV003012167
dbSNP Id:
rs878854126
gnomAD v4:
3-10149830-A-G
MyVariant Identifiers:
chr3:g.10191514A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10149830A>G , CM000665.2:g.10149830A>G | GRCh38 |
| NC_000003.11:g.10191514A>G , CM000665.1:g.10191514A>G | GRCh37 |
| NC_000003.10:g.10166514A>G | NCBI36 |
| NG_008212.3:g.13196A>G , LRG_322:g.13196A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696142.1:c.*184A>G | ENSP00000512434.1:n.*184A>G | |
| ENST00000696143.1:c.643A>G | ENSP00000512435.1:n.643A>G | |
| ENST00000696153.1:c.618A>G | ENSP00000512444.1:p.Leu206= | |
| ENST00000256474.3:c.507A>G MANE Select | ENSP00000256474.3:p.Leu169= | |
| ENST00000256474.2:c.507A>G | ENSP00000256474.2:p.Leu169= | |
| ENST00000345392.2:c.384A>G | ENSP00000344757.2:p.Leu128= | |
| ENST00000477538.1:n.643A>G | ||
| NM_000551.3:c.507A>G , LRG_322t1:c.507A>G | NP_000542.1:p.Leu169= | |
| NM_198156.2:c.384A>G | NP_937799.1:p.Leu128= | |
| NM_001354723.1:c.*61A>G | NP_001341652.1:n.*61A>G | |
| NM_000551.4:c.507A>G MANE Select | NP_000542.1:p.Leu169= | |
| NM_001354723.2:c.*61A>G | NP_001341652.1:n.*61A>G | |
| NM_198156.3:c.384A>G | NP_937799.1:p.Leu128= |