Linked Data
dbSNP Id:
rs1932575866
gnomAD v3:
22-42132658-G-T
gnomAD v4:
22-42132658-G-T
MyVariant Identifiers:
chr22:g.42528665G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.42132658G>T , CM000684.2:g.42132658G>T | GRCh38 |
| NC_000022.10:g.42528665G>T , CM000684.1:g.42528665G>T | GRCh37 |
| NC_000022.9:g.40858609G>T | NCBI36 |
| NG_008376.3:g.2334C>A | |
| NG_008376.4:g.3153C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000417586.1:n.116G>T | ||
| XM_011529967.1:c.-1045-822C>A | XP_011528269.1:n.-1045-822C>A |