Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.137192182T>C , CM000671.2:g.137192182T>C | GRCh38 |
| NC_000009.11:g.140086634T>C , CM000671.1:g.140086634T>C | GRCh37 |
| NC_000009.10:g.139206455T>C | NCBI36 |
| NG_027801.1:g.13530A>G | |
| NG_027801.2:g.17012A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409012.6:c.2074-8A>G MANE Select | ENSP00000387100.4:n.2074-8A>G | |
| ENST00000333046.8:c.1544A>G | ENSP00000327617.4:p.His515Arg | |
| ENST00000409012.4:c.2074-8A>G | ENSP00000387100.4:n.2074-8A>G | |
| ENST00000477345.1:n.2795-8A>G | ||
| NM_001128228.2:c.2074-8A>G | NP_001121700.2:n.2074-8A>G | |
| NM_001128228.3:c.2074-8A>G MANE Select | NP_001121700.2:n.2074-8A>G |