Linked Data
MyVariant Identifiers:
chr2:g.189923599T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189058873T>A , CM000664.2:g.189058873T>A | GRCh38 |
| NC_000002.11:g.189923599T>A , CM000664.1:g.189923599T>A | GRCh37 |
| NC_000002.10:g.189631844T>A | NCBI36 |
| NG_011799.1:g.126007A>T | |
| NG_011799.2:g.126007A>T | |
| NG_011799.3:g.171429A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374866.9:c.2106A>T MANE Select | ENSP00000364000.3:p.Gly702= | |
| ENST00000374866.7:c.2106A>T | ENSP00000364000.3:p.Gly702= | |
| ENST00000470524.2:n.212A>T | ||
| ENST00000618828.1:c.945A>T | ENSP00000482184.1:p.Gly315= | |
| NM_000393.3:c.2106A>T | NP_000384.2:p.Gly702= | |
| XM_011510573.1:c.1968A>T | XP_011508875.1:p.Gly656= | |
| NM_000393.4:c.2106A>T | NP_000384.2:p.Gly702= | |
| XM_011510573.3:c.1968A>T | XP_011508875.1:p.Gly656= | |
| NM_000393.5:c.2106A>T MANE Select | NP_000384.2:p.Gly702= |