Linked Data
MyVariant Identifiers:
chr11:g.55579470C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.55811994C>T , CM000673.2:g.55811994C>T | GRCh38 |
| NC_000011.9:g.55579470C>T , CM000673.1:g.55579470C>T | GRCh37 |
| NC_000011.8:g.55336046C>T | NCBI36 |
| NG_052620.1:g.5628C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000625203.2:c.528C>T MANE Select | ENSP00000485319.1:p.His176= | |
| ENST00000333973.3:c.528C>T | ENSP00000335529.2:p.His176= | |
| ENST00000623450.1:c.528C>T | ENSP00000485509.1:p.His176= | |
| ENST00000625203.1:c.528C>T | ENSP00000485319.1:p.His176= | |
| NM_001004738.1:c.528C>T | NP_001004738.1:p.His176= | |
| NM_001004738.2:c.528C>T MANE Select | NP_001004738.1:p.His176= |