Linked Data
gnomAD v4:
11-67583621-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67583621C>A , CM000673.2:g.67583621C>A | GRCh38 |
| NC_000011.9:g.67351092C>A , CM000673.1:g.67351092C>A | GRCh37 |
| NC_000011.8:g.67107668C>A | NCBI36 |
| NG_012075.1:g.5027C>A , LRG_723:g.5027C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398606.7:c.-223C>A | ENSP00000381607.3:n.-223C>A | |
| NM_000852.3:c.-223C>A , LRG_723t1:c.-223C>A | NP_000843.1:n.-223C>A |