Linked Data
MyVariant Identifiers:
chr22:g.27003883A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.26607919A>G , CM000684.2:g.26607919A>G | GRCh38 |
| NC_000022.10:g.27003883A>G , CM000684.1:g.27003883A>G | GRCh37 |
| NC_000022.9:g.25333883A>G | NCBI36 |
| NG_009826.1:g.15109T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647569.1:n.214T>C | ||
| ENST00000647684.1:c.402T>C MANE Select | ENSP00000497249.1:p.Asp134= | |
| ENST00000215939.2:c.402T>C | ENSP00000215939.2:p.Asp134= | |
| NM_001887.3:c.402T>C | NP_001878.1:p.Asp134= | |
| XM_011529899.1:c.402T>C | XP_011528201.1:p.Asp134= | |
| NM_001887.4:c.402T>C MANE Select | NP_001878.1:p.Asp134= | |
| XM_011529899.3:c.402T>C | XP_011528201.1:p.Asp134= |