Linked Data
dbSNP Id:
rs2071224599
gnomAD v3:
3-142470090-T-C
gnomAD v4:
3-142470090-T-C
MyVariant Identifiers:
chr3:g.142188932T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.142470090T>C , CM000665.2:g.142470090T>C | GRCh38 |
| NC_000003.11:g.142188932T>C , CM000665.1:g.142188932T>C | GRCh37 |
| NC_000003.10:g.143671622T>C | NCBI36 |
| NG_008951.1:g.113737A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000350721.9:c.6315A>G MANE Select | ENSP00000343741.4:p.Glu2105= | |
| ENST00000513291.2:n.1499A>G | ||
| ENST00000654170.1:n.1158A>G | ||
| ENST00000656590.1:c.5105A>G | ||
| ENST00000661310.1:c.6123A>G | ENSP00000499589.1:p.Glu2041= | |
| ENST00000665483.1:n.170A>G | ||
| ENST00000666447.1:n.150A>G | ||
| ENST00000666943.1:n.1779A>G | ||
| ENST00000350721.8:c.6315A>G | ENSP00000343741.4:p.Glu2105= | |
| NM_001184.3:c.6315A>G | NP_001175.2:p.Glu2105= | |
| XM_011512924.1:c.6321A>G | XP_011511226.1:p.Glu2107= | |
| XM_011512925.1:c.6129A>G | XP_011511227.1:p.Glu2043= | |
| XR_924147.1:n.6410A>G | ||
| XR_924148.1:n.6410A>G | ||
| XR_924149.1:n.6289A>G | ||
| NM_001354579.1:c.6123A>G | NP_001341508.1:p.Glu2041= | |
| XR_001740179.2:n.6404A>G | ||
| XR_001740180.2:n.6458A>G | ||
| XR_001740181.2:n.6337A>G | ||
| XR_001740182.1:n.6289A>G | ||
| XR_002959543.1:n.6514A>G | ||
| XR_924148.2:n.6410A>G | ||
| NM_001184.4:c.6315A>G MANE Select | NP_001175.2:p.Glu2105= | |
| NM_001354579.2:c.6123A>G | NP_001341508.1:p.Glu2041= |