Linked Data
MyVariant Identifiers:
chr1:g.198867691T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.198898562T>C , CM000663.2:g.198898562T>C | GRCh38 |
| NC_000001.10:g.198867691T>C , CM000663.1:g.198867691T>C | GRCh37 |
| NC_000001.9:g.197134314T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_040073.1:n.363+1849A>G |