Linked Data
dbSNP Id:
rs1234425654
gnomAD v3:
22-42132618-GCTGC-G
gnomAD v4:
22-42132618-GCTGC-G
MyVariant Identifiers:
chr22:g.42132619_42132622del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.42132620_42132623del , CM000684.2:g.42132620_42132623del | GRCh38 |
| NC_000022.10:g.42528627_42528630del , CM000684.1:g.42528627_42528630del | GRCh37 |
| NC_000022.9:g.40858571_40858574del | NCBI36 |
| NG_008376.3:g.2370_2373del | |
| NG_008376.4:g.3189_3192del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000417586.1:n.78_81del | ||
| XM_011529967.1:c.-1045-786_-1045-783del | XP_011528269.1:n.-1045-786_-1045-783del |