Linked Data
MyVariant Identifiers:
chr11:g.55579506T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.55812030T>C , CM000673.2:g.55812030T>C | GRCh38 |
| NC_000011.9:g.55579506T>C , CM000673.1:g.55579506T>C | GRCh37 |
| NC_000011.8:g.55336082T>C | NCBI36 |
| NG_052620.1:g.5664T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000625203.2:c.564T>C MANE Select | ENSP00000485319.1:p.Ala188= | |
| ENST00000333973.3:c.564T>C | ENSP00000335529.2:p.Ala188= | |
| ENST00000623450.1:c.564T>C | ENSP00000485509.1:p.Ala188= | |
| ENST00000625203.1:c.564T>C | ENSP00000485319.1:p.Ala188= | |
| NM_001004738.1:c.564T>C | NP_001004738.1:p.Ala188= | |
| NM_001004738.2:c.564T>C MANE Select | NP_001004738.1:p.Ala188= |