Linked Data
MyVariant Identifiers:
chr2:g.189915325C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189050599C>T , CM000664.2:g.189050599C>T | GRCh38 |
| NC_000002.11:g.189915325C>T , CM000664.1:g.189915325C>T | GRCh37 |
| NC_000002.10:g.189623570C>T | NCBI36 |
| NG_011799.1:g.134281G>A | |
| NG_011799.2:g.134281G>A | |
| NG_011799.3:g.179703G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374866.9:c.3009G>A MANE Select | ENSP00000364000.3:p.Glu1003= | |
| ENST00000374866.7:c.3009G>A | ENSP00000364000.3:p.Glu1003= | |
| ENST00000618828.1:c.1848G>A | ENSP00000482184.1:p.Glu616= | |
| NM_000393.3:c.3009G>A | NP_000384.2:p.Glu1003= | |
| XM_011510573.1:c.2871G>A | XP_011508875.1:p.Glu957= | |
| NM_000393.4:c.3009G>A | NP_000384.2:p.Glu1003= | |
| XM_011510573.3:c.2871G>A | XP_011508875.1:p.Glu957= | |
| NM_000393.5:c.3009G>A MANE Select | NP_000384.2:p.Glu1003= |