Linked Data
gnomAD v4:
11-47331770-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.47331770T>C , CM000673.2:g.47331770T>C | GRCh38 |
| NC_000011.9:g.47353321T>C , CM000673.1:g.47353321T>C | GRCh37 |
| NC_000011.8:g.47309897T>C | NCBI36 |
| NG_007667.1:g.25933A>G , LRG_386:g.25933A>G | |
| NG_029462.1:g.67395T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000545968.6:c.*27-54A>G MANE Select | ENSP00000442795.1:n.*27-54A>G | |
| ENST00000256993.8:c.*27-54A>G | ENSP00000256993.5:n.*27-54A>G | |
| ENST00000399249.6:c.*27-54A>G | ENSP00000382193.2:n.*27-54A>G | |
| ENST00000545968.5:c.*27-54A>G | ENSP00000442795.1:n.*27-54A>G | |
| NM_000256.3:c.*27-54A>G , LRG_386t1:c.*27-54A>G MANE Select | NP_000247.2:n.*27-54A>G | |
| XM_011520117.1:c.*27-54A>G | XP_011518419.1:n.*27-54A>G | |
| XM_011520118.1:c.*27-54A>G | XP_011518420.1:n.*27-54A>G |