Linked Data
gnomAD v4:
6-3154618-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3154618T>C , CM000668.2:g.3154618T>C | GRCh38 |
| NC_000006.11:g.3154852T>C , CM000668.1:g.3154852T>C | GRCh37 |
| NC_000006.10:g.3099851T>C | NCBI36 |
| NG_042223.1:g.7932A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333628.4:c.583A>G MANE Select | ENSP00000369703.2:p.Asn195Asp | |
| ENST00000679400.1:n.639A>G | ||
| ENST00000679907.1:n.971A>G | ||
| ENST00000680036.1:n.1365A>G | ||
| ENST00000680967.1:n.1673A>G | ||
| ENST00000333628.3:c.583A>G | ENSP00000369703.2:p.Asn195Asp | |
| ENST00000489942.1:n.778A>G | ||
| NM_001069.2:c.583A>G | NP_001060.1:p.Asn195Asp | |
| NM_001310315.1:c.328A>G | NP_001297244.1:p.Asn110Asp | |
| NM_001069.3:c.583A>G MANE Select | NP_001060.1:p.Asn195Asp | |
| NM_001310315.2:c.328A>G | NP_001297244.1:p.Asn110Asp |