Linked Data
MyVariant Identifiers:
chr2:g.215675014G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.214810290G>C , CM000664.2:g.214810290G>C | GRCh38 |
| NC_000002.11:g.215675014G>C , CM000664.1:g.215675014G>C | GRCh37 |
| NC_000002.10:g.215383259G>C | NCBI36 |
| NG_012047.2:g.4415C>G | |
| NG_012047.3:g.4422C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_110292.1:n.62G>C |