Linked Data
gnomAD v4:
22-42132387-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.42132387G>T , CM000684.2:g.42132387G>T | GRCh38 |
| NC_000022.10:g.42528394G>T , CM000684.1:g.42528394G>T | GRCh37 |
| NC_000022.9:g.40858338G>T | NCBI36 |
| NG_008376.3:g.2605C>A | |
| NG_008376.4:g.3424C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XM_011529967.1:c.-1045-551C>A | XP_011528269.1:n.-1045-551C>A |