Linked Data
gnomAD v4:
22-23786960-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.23786960G>T , CM000684.2:g.23786960G>T | GRCh38 |
| NC_000022.10:g.24129147G>T , CM000684.1:g.24129147G>T | GRCh37 |
| NC_000022.9:g.22459147G>T | NCBI36 |
| NG_009303.1:g.4998G>T , LRG_520:g.4998G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000407422.8:c.-210G>T | ENSP00000383984.3:n.-210G>T | |
| NM_001007468.2:c.-210G>T | NP_001007469.1:n.-210G>T | |
| NM_001317946.1:c.-210G>T | NP_001304875.1:n.-210G>T | |
| NM_001362877.1:c.-210G>T | NP_001349806.1:n.-210G>T | |
| NM_003073.4:c.-210G>T | NP_003064.2:n.-210G>T |