Linked Data
gnomAD v4:
20-35438351-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.35438351A>C , CM000682.2:g.35438351A>C | GRCh38 |
| NC_000020.10:g.34026131A>C , CM000682.1:g.34026131A>C | GRCh37 |
| NC_000020.9:g.33489545A>C | NCBI36 |
| NG_008076.2:g.4869T>G | |
| NG_008076.3:g.21396T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374372.1:c.-241-182T>G | ENSP00000363492.1:n.-241-182T>G | |
| XM_011529075.1:c.-241-182T>G | XP_011527377.1:n.-241-182T>G | |
| XM_011529076.1:c.-241-182T>G | XP_011527378.1:n.-241-182T>G | |
| NM_001319138.1:c.-241-182T>G | NP_001306067.1:n.-241-182T>G | |
| NM_001319138.2:c.-241-182T>G | NP_001306067.1:n.-241-182T>G |