Linked Data
MyVariant Identifiers:
chr2:g.189923578A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189058852A>T , CM000664.2:g.189058852A>T | GRCh38 |
| NC_000002.11:g.189923578A>T , CM000664.1:g.189923578A>T | GRCh37 |
| NC_000002.10:g.189631823A>T | NCBI36 |
| NG_011799.1:g.126028T>A | |
| NG_011799.2:g.126028T>A | |
| NG_011799.3:g.171450T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374866.9:c.2127T>A MANE Select | ENSP00000364000.3:p.Pro709= | |
| ENST00000374866.7:c.2127T>A | ENSP00000364000.3:p.Pro709= | |
| ENST00000470524.2:n.233T>A | ||
| ENST00000618828.1:c.966T>A | ENSP00000482184.1:p.Pro322= | |
| NM_000393.3:c.2127T>A | NP_000384.2:p.Pro709= | |
| XM_011510573.1:c.1989T>A | XP_011508875.1:p.Pro663= | |
| NM_000393.4:c.2127T>A | NP_000384.2:p.Pro709= | |
| XM_011510573.3:c.1989T>A | XP_011508875.1:p.Pro663= | |
| NM_000393.5:c.2127T>A MANE Select | NP_000384.2:p.Pro709= |