Linked Data
MyVariant Identifiers:
chr8:g.38001866G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.38144348G>C , CM000670.2:g.38144348G>C | GRCh38 |
| NC_000008.10:g.38001866G>C , CM000670.1:g.38001866G>C | GRCh37 |
| NC_000008.9:g.38121023G>C | NCBI36 |
| NG_011827.1:g.11735C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000276449.9:c.783C>G MANE Select | ENSP00000276449.3:p.Ser261= | |
| ENST00000276449.8:c.783C>G | ENSP00000276449.3:p.Ser261= | |
| ENST00000520114.1:n.2752C>G | ||
| ENST00000522050.1:c.625C>G | ||
| NM_000349.2:c.783C>G | NP_000340.2:p.Ser261= | |
| XM_006716392.1:c.689C>G | XP_006716455.1:p.Pro230Arg | |
| NM_000349.3:c.783C>G MANE Select | NP_000340.2:p.Ser261= |