Linked Data
MyVariant Identifiers:
chr11:g.64518888G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.64751416G>C , CM000673.2:g.64751416G>C | GRCh38 |
| NC_000011.9:g.64518888G>C , CM000673.1:g.64518888G>C | GRCh37 |
| NC_000011.8:g.64275464G>C | NCBI36 |
| NG_013018.1:g.14300C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000164139.4:c.1878C>G MANE Select | ENSP00000164139.3:p.Ala626= | |
| ENST00000164139.3:c.1878C>G | ENSP00000164139.3:p.Ala626= | |
| ENST00000377432.7:c.1614C>G | ENSP00000366650.3:p.Ala538= | |
| ENST00000462303.1:n.202C>G | ||
| NM_001164716.1:c.1614C>G | NP_001158188.1:p.Ala538= | |
| NM_005609.2:c.1878C>G | NP_005600.1:p.Ala626= | |
| NM_005609.3:c.1878C>G | NP_005600.1:p.Ala626= | |
| NM_005609.4:c.1878C>G MANE Select | NP_005600.1:p.Ala626= |