Linked Data
MyVariant Identifiers:
chr2:g.219678887A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218814164A>G , CM000664.2:g.218814164A>G | GRCh38 |
| NC_000002.11:g.219678887A>G , CM000664.1:g.219678887A>G | GRCh37 |
| NC_000002.10:g.219387131A>G | NCBI36 |
| NG_007959.1:g.37416A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258415.9:c.1161A>G MANE Select | ENSP00000258415.4:p.Lys387= | |
| ENST00000258415.8:c.1161A>G | ENSP00000258415.4:p.Lys387= | |
| ENST00000494263.5:n.1595A>G | ||
| NM_000784.3:c.1161A>G | NP_000775.1:p.Lys387= | |
| XM_017003488.2:c.741A>G | XP_016858977.1:p.Lys247= | |
| NM_000784.4:c.1161A>G MANE Select | NP_000775.1:p.Lys387= |