Linked Data
MyVariant Identifiers:
chr2:g.241522274T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240582857T>C , CM000664.2:g.240582857T>C | GRCh38 |
| NC_000002.11:g.241522274T>C , CM000664.1:g.241522274T>C | GRCh37 |
| NC_000002.10:g.241170947T>C | NCBI36 |
| NG_011558.2:g.1142T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_103792.1:n.3460A>G |