Linked Data
gnomAD v4:
11-2444922-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2444922A>G , CM000673.2:g.2444922A>G | GRCh38 |
| NC_000011.9:g.2466152A>G , CM000673.1:g.2466152A>G | GRCh37 |
| NC_000011.8:g.2422728A>G | NCBI36 |
| NG_008935.1:g.4932A>G , LRG_287:g.4932A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496887.7:c.23+214A>G | ENSP00000434560.2:n.23+214A>G | |
| ENST00000496887.6:c.23+214A>G | ENSP00000434560.1:n.23+214A>G |