Linked Data
MyVariant Identifiers:
chr2:g.219746904G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218882182G>A , CM000664.2:g.218882182G>A | GRCh38 |
| NC_000002.11:g.219746904G>A , CM000664.1:g.219746904G>A | GRCh37 |
| NC_000002.10:g.219455148G>A | NCBI36 |
| NG_012179.1:g.6650G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258411.8:c.135G>A MANE Select | ENSP00000258411.3:p.Leu45= | |
| ENST00000258411.7:c.135G>A | ENSP00000258411.3:p.Leu45= | |
| ENST00000458582.1:c.22G>A | ||
| NM_025216.2:c.135G>A | NP_079492.2:p.Leu45= | |
| XM_011511928.1:c.84G>A | XP_011510230.1:p.Leu28= | |
| XM_011511929.1:c.39G>A | XP_011510231.1:p.Leu13= | |
| XM_011511930.1:c.135G>A | XP_011510232.1:p.Leu45= | |
| XM_011511929.2:c.39G>A | XP_011510231.1:p.Leu13= | |
| NM_025216.3:c.135G>A MANE Select | NP_079492.2:p.Leu45= |