Linked Data
MyVariant Identifiers:
chr2:g.215674996G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.214810272G>A , CM000664.2:g.214810272G>A | GRCh38 |
| NC_000002.11:g.215674996G>A , CM000664.1:g.215674996G>A | GRCh37 |
| NC_000002.10:g.215383241G>A | NCBI36 |
| NG_012047.2:g.4433C>T | |
| NG_012047.3:g.4440C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_110292.1:n.44G>A |