Linked Data
MyVariant Identifiers:
chr22:g.42528770T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.42132763T>G , CM000684.2:g.42132763T>G | GRCh38 |
| NC_000022.10:g.42528770T>G , CM000684.1:g.42528770T>G | GRCh37 |
| NC_000022.9:g.40858714T>G | NCBI36 |
| NG_008376.3:g.2229A>C | |
| NG_008376.4:g.3048A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000417586.1:n.221T>G | ||
| XM_011529967.1:c.-1045-927A>C | XP_011528269.1:n.-1045-927A>C |