Linked Data
MyVariant Identifiers:
chr4:g.69512852G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.68647134G>C , CM000666.2:g.68647134G>C | GRCh38 |
| NC_000004.11:g.69512852G>C , CM000666.1:g.69512852G>C | GRCh37 |
| NC_000004.10:g.69195447G>C | NCBI36 |
| NG_052676.1:g.28643C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338206.6:c.1563C>G MANE Select | ENSP00000341045.5:p.Ala521= | |
| ENST00000338206.5:c.1563C>G | ENSP00000341045.5:p.Ala521= | |
| ENST00000616841.4:c.1563C>G | ENSP00000482004.1:p.Ala521= | |
| NM_001076.3:c.1563C>G | NP_001067.2:p.Ala521= | |
| NM_001076.4:c.1563C>G MANE Select | NP_001067.2:p.Ala521= |