Linked Data
MyVariant Identifiers:
chr21:g.33031712T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.31659399T>A , CM000683.2:g.31659399T>A | GRCh38 |
| NC_000021.8:g.33031712T>A , CM000683.1:g.33031712T>A | GRCh37 |
| NC_000021.7:g.31953583T>A | NCBI36 |
| NG_008689.1:g.4778T>A , LRG_652:g.4778T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_430363.2:n.122A>T | ||
| XR_937662.1:n.122A>T | ||
| XR_002958653.1:n.86A>T | ||
| XR_430363.3:n.157A>T |