Linked Data
MyVariant Identifiers:
chr11:g.66328058G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.66560587G>C , CM000673.2:g.66560587G>C | GRCh38 |
| NC_000011.9:g.66328058G>C , CM000673.1:g.66328058G>C | GRCh37 |
| NC_000011.8:g.66084634G>C | NCBI36 |
| NG_013304.2:g.18668G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000513398.2:c.1692G>C MANE Select | ENSP00000426797.1:p.Ala564= | |
| ENST00000502692.5:c.1821G>C | ENSP00000422007.1:p.Ala607= | |
| ENST00000513398.1:c.1692G>C | ENSP00000426797.1:p.Ala564= | |
| NM_001104.3:c.1692G>C | NP_001095.2:p.Ala564= | |
| NM_001258371.2:c.1821G>C | NP_001245300.2:p.Ala607= | |
| NM_001104.4:c.1692G>C MANE Select | NP_001095.2:p.Ala564= | |
| NM_001258371.3:c.1821G>C | NP_001245300.2:p.Ala607= |