Linked Data
dbSNP Id:
rs1932597690
gnomAD v4:
22-42132726-A-T
MyVariant Identifiers:
chr22:g.42528733A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.42132726A>T , CM000684.2:g.42132726A>T | GRCh38 |
| NC_000022.10:g.42528733A>T , CM000684.1:g.42528733A>T | GRCh37 |
| NC_000022.9:g.40858677A>T | NCBI36 |
| NG_008376.3:g.2266T>A | |
| NG_008376.4:g.3085T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000417586.1:n.184A>T | ||
| XM_011529967.1:c.-1045-890T>A | XP_011528269.1:n.-1045-890T>A |