Linked Data
MyVariant Identifiers:
chr6:g.28129594A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.28161816A>T , CM000668.2:g.28161816A>T | GRCh38 |
| NC_000006.11:g.28129594A>T , CM000668.1:g.28129594A>T | GRCh37 |
| NC_000006.10:g.28237573A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000562227.2:n.48A>T | ||
| ENST00000440790.6:n.36A>T | ||
| ENST00000570126.1:n.25A>T | ||
| NR_103448.1:n.56A>T |