Linked Data
gnomAD v4:
X-101348886-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.101348886T>G , CM000685.2:g.101348886T>G | GRCh38 |
| NC_000023.10:g.100603874T>G , CM000685.1:g.100603874T>G | GRCh37 |
| NC_000023.9:g.100490530T>G | NCBI36 |
| NG_009616.1:g.42339A>C , LRG_128:g.42339A>C | |
| NG_011734.1:g.5084A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372902.3:c.-222A>C | ENSP00000361993.3:n.-222A>C | |
| NM_004085.3:c.-222A>C | NP_004076.1:n.-222A>C |