Linked Data
gnomAD v4:
22-42132295-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.42132295T>C , CM000684.2:g.42132295T>C | GRCh38 |
| NC_000022.10:g.42528302T>C , CM000684.1:g.42528302T>C | GRCh37 |
| NC_000022.9:g.40858246T>C | NCBI36 |
| NG_008376.3:g.2697A>G | |
| NG_008376.4:g.3516A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XM_011529967.1:c.-1045-459A>G | XP_011528269.1:n.-1045-459A>G |