Linked Data
MyVariant Identifiers:
chr2:g.136547226T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.135789656T>A , CM000664.2:g.135789656T>A | GRCh38 |
| NC_000002.11:g.136547226T>A , CM000664.1:g.136547226T>A | GRCh37 |
| NC_000002.10:g.136263696T>A | NCBI36 |
| NG_008104.2:g.70514A>T , LRG_338:g.70514A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264162.7:c.5478A>T MANE Select | ENSP00000264162.2:p.Ala1826= | |
| ENST00000264162.6:c.5478A>T | ENSP00000264162.2:p.Ala1826= | |
| NM_002299.2:c.5478A>T , LRG_338t1:c.5478A>T | NP_002290.2:p.Ala1826= | |
| NM_002299.3:c.5478A>T | NP_002290.2:p.Ala1826= | |
| NM_002299.4:c.5478A>T MANE Select | NP_002290.2:p.Ala1826= |