Linked Data
dbSNP Id:
rs1466070519
gnomAD v3:
22-42132452-T-G
gnomAD v4:
22-42132452-T-G
MyVariant Identifiers:
chr22:g.42132452T>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.42132452T>G , CM000684.2:g.42132452T>G | GRCh38 |
| NC_000022.10:g.42528459T>G , CM000684.1:g.42528459T>G | GRCh37 |
| NC_000022.9:g.40858403T>G | NCBI36 |
| NG_008376.3:g.2540A>C | |
| NG_008376.4:g.3359A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011529967.1:c.-1045-616A>C | XP_011528269.1:n.-1045-616A>C |