Linked Data
MyVariant Identifiers:
chr4:g.186065920C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.185144766C>T , CM000666.2:g.185144766C>T | GRCh38 |
| NC_000004.11:g.186065920C>T , CM000666.1:g.186065920C>T | GRCh37 |
| NC_000004.10:g.186302914C>T | NCBI36 |
| NG_013001.1:g.6504C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000281456.11:c.114C>T MANE Select | ENSP00000281456.5:p.Val38= | |
| ENST00000281456.10:c.114C>T | ENSP00000281456.5:p.Val38= | |
| ENST00000491736.1:c.114C>T | ENSP00000476711.1:p.Val38= | |
| NM_001151.3:c.114C>T | NP_001142.2:p.Val38= | |
| NM_001151.4:c.114C>T MANE Select | NP_001142.2:p.Val38= |