Linked Data
MyVariant Identifiers:
chr2:g.241522272G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240582855G>C , CM000664.2:g.240582855G>C | GRCh38 |
| NC_000002.11:g.241522272G>C , CM000664.1:g.241522272G>C | GRCh37 |
| NC_000002.10:g.241170945G>C | NCBI36 |
| NG_011558.2:g.1140G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_103792.1:n.3462C>G |