Linked Data
gnomAD v4:
11-86954651-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.86954651T>C , CM000673.2:g.86954651T>C | GRCh38 |
| NC_000011.9:g.86665693T>C , CM000673.1:g.86665693T>C | GRCh37 |
| NC_000011.8:g.86343341T>C | NCBI36 |
| NG_011752.1:g.5741A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000531380.2:c.285+150A>G MANE Select | ENSP00000434034.1:n.285+150A>G | |
| ENST00000531380.1:c.285+150A>G | ENSP00000434034.1:n.285+150A>G | |
| NM_012193.3:c.285+150A>G | NP_036325.2:n.285+150A>G | |
| NM_012193.4:c.285+150A>G MANE Select | NP_036325.2:n.285+150A>G |