Linked Data
gnomAD v4:
22-41621081-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.41621081C>T , CM000684.2:g.41621081C>T | GRCh38 |
| NC_000022.10:g.42017085C>T , CM000684.1:g.42017085C>T | GRCh37 |
| NC_000022.9:g.40347031C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263256.6:c.-242G>A | ENSP00000263256.6:n.-242G>A |