Linked Data
MyVariant Identifiers:
chr2:g.241522258C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240582841C>T , CM000664.2:g.240582841C>T | GRCh38 |
| NC_000002.11:g.241522258C>T , CM000664.1:g.241522258C>T | GRCh37 |
| NC_000002.10:g.241170931C>T | NCBI36 |
| NG_011558.2:g.1126C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_103792.1:n.3476G>A |