Linked Data
MyVariant Identifiers:
chr2:g.241522198T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240582781T>A , CM000664.2:g.240582781T>A | GRCh38 |
| NC_000002.11:g.241522198T>A , CM000664.1:g.241522198T>A | GRCh37 |
| NC_000002.10:g.241170871T>A | NCBI36 |
| NG_011558.2:g.1066T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_103792.1:n.3536A>T |