Linked Data
MyVariant Identifiers:
chr4:g.103422462T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.102501305T>A , CM000666.2:g.102501305T>A | GRCh38 |
| NC_000004.11:g.103422462T>A , CM000666.1:g.103422462T>A | GRCh37 |
| NC_000004.10:g.103641494T>A | NCBI36 |
| NG_050628.1:g.4977T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011532467.1:c.587A>T | XP_011530769.1:p.Asp196Val | |
| NR_136202.1:n.48+1134A>T | ||
| XM_024454067.1:c.-537T>A | XP_024309835.1:n.-537T>A | |
| XM_024454069.1:c.-537T>A | XP_024309837.1:n.-537T>A |