Linked Data
gnomAD v4:
X-101348872-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.101348872A>C , CM000685.2:g.101348872A>C | GRCh38 |
| NC_000023.10:g.100603860A>C , CM000685.1:g.100603860A>C | GRCh37 |
| NC_000023.9:g.100490516A>C | NCBI36 |
| NG_009616.1:g.42353T>G , LRG_128:g.42353T>G | |
| NG_011734.1:g.5098T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372902.3:c.-208T>G | ENSP00000361993.3:n.-208T>G | |
| NM_004085.3:c.-208T>G | NP_004076.1:n.-208T>G |