Linked Data
MyVariant Identifiers:
chr2:g.176958353C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.176093625C>G , CM000664.2:g.176093625C>G | GRCh38 |
| NC_000002.11:g.176958353C>G , CM000664.1:g.176958353C>G | GRCh37 |
| NC_000002.10:g.176666599C>G | NCBI36 |
| NG_008137.1:g.5822C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392539.4:c.735C>G MANE Select | ENSP00000376322.3:p.Thr245= | |
| ENST00000392539.3:c.735C>G | ENSP00000376322.3:p.Thr245= | |
| NM_000523.3:c.735C>G | NP_000514.2:p.Thr245= | |
| XM_011511068.1:c.725-855C>G | XP_011509370.1:n.725-855C>G | |
| XM_011511068.2:c.725-855C>G | XP_011509370.1:n.725-855C>G | |
| NM_000523.4:c.735C>G MANE Select | NP_000514.2:p.Thr245= |