Linked Data
MyVariant Identifiers:
chr1:g.186650339C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186681207C>T , CM000663.2:g.186681207C>T | GRCh38 |
| NC_000001.10:g.186650339C>T , CM000663.1:g.186650339C>T | GRCh37 |
| NC_000001.9:g.184916962C>T | NCBI36 |
| NG_028206.2:g.4221G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_125801.1:n.554C>T |