Linked Data
MyVariant Identifiers:
chr22:g.42528775C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.42132768C>A , CM000684.2:g.42132768C>A | GRCh38 |
| NC_000022.10:g.42528775C>A , CM000684.1:g.42528775C>A | GRCh37 |
| NC_000022.9:g.40858719C>A | NCBI36 |
| NG_008376.3:g.2224G>T | |
| NG_008376.4:g.3043G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000417586.1:n.226C>A | ||
| XM_011529967.1:c.-1045-932G>T | XP_011528269.1:n.-1045-932G>T |