Linked Data
gnomAD v4:
11-68685551-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.68685551C>G , CM000673.2:g.68685551C>G | GRCh38 |
| NC_000011.9:g.68453019C>G , CM000673.1:g.68453019C>G | GRCh37 |
| NC_000011.8:g.68209595C>G | NCBI36 |
| NG_052785.1:g.6077C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265643.4:c.82-43C>G MANE Select | ENSP00000265643.3:n.82-43C>G | |
| ENST00000265643.3:c.82-43C>G | ENSP00000265643.3:n.82-43C>G | |
| NM_015973.3:c.82-43C>G | NP_057057.2:n.82-43C>G | |
| NM_015973.4:c.82-43C>G | NP_057057.2:n.82-43C>G | |
| XR_001748281.1:n.230+2290G>C | ||
| NM_015973.5:c.82-43C>G MANE Select | NP_057057.2:n.82-43C>G |