Linked Data
MyVariant Identifiers:
chr22:g.42528560G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.42132553G>C , CM000684.2:g.42132553G>C | GRCh38 |
| NC_000022.10:g.42528560G>C , CM000684.1:g.42528560G>C | GRCh37 |
| NC_000022.9:g.40858504G>C | NCBI36 |
| NG_008376.3:g.2439C>G | |
| NG_008376.4:g.3258C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000417586.1:n.11G>C | ||
| XM_011529967.1:c.-1045-717C>G | XP_011528269.1:n.-1045-717C>G |