Linked Data
gnomAD v4:
20-46011439-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46011439A>G , CM000682.2:g.46011439A>G | GRCh38 |
| NC_000020.10:g.44640078A>G , CM000682.1:g.44640078A>G | GRCh37 |
| NC_000020.9:g.44073485A>G | NCBI36 |
| NG_011468.1:g.7532A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372330.3:c.823+123A>G MANE Select | ENSP00000361405.3:n.823+123A>G | |
| NM_004994.2:c.823+123A>G | NP_004985.2:n.823+123A>G | |
| NM_004994.3:c.823+123A>G MANE Select | NP_004985.2:n.823+123A>G |