Linked Data
MyVariant Identifiers:
chr2:g.241522206C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240582789C>G , CM000664.2:g.240582789C>G | GRCh38 |
| NC_000002.11:g.241522206C>G , CM000664.1:g.241522206C>G | GRCh37 |
| NC_000002.10:g.241170879C>G | NCBI36 |
| NG_011558.2:g.1074C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_103792.1:n.3528G>C |