Linked Data
MyVariant Identifiers:
chr2:g.5832937T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.5692805T>G , CM000664.2:g.5692805T>G | GRCh38 |
| NC_000002.11:g.5832937T>G , CM000664.1:g.5832937T>G | GRCh37 |
| NC_000002.10:g.5750388T>G | NCBI36 |
| NG_050751.1:g.5139T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000322002.5:c.84T>G MANE Select | ENSP00000322568.3:p.Ala28= | |
| ENST00000322002.4:c.84T>G | ENSP00000322568.3:p.Ala28= | |
| NM_003108.3:c.84T>G | NP_003099.1:p.Ala28= | |
| NM_003108.4:c.84T>G MANE Select | NP_003099.1:p.Ala28= |