Linked Data
MyVariant Identifiers:
chr6:g.29760362G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.29792585G>C , CM000668.2:g.29792585G>C | GRCh38 |
| NC_000006.11:g.29760362G>C , CM000668.1:g.29760362G>C | GRCh37 |
| NC_000006.10:g.29868341G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000418983.1:n.166C>G (HCG4) | ||
| ENST00000429037.2:n.221G>C (HLA-V) | ||
| ENST00000446817.1:n.331G>C (HLA-V) | ||
| ENST00000457107.5:n.232G>C (HLA-V) | ||
| ENST00000476601.5:n.549G>C (HLA-V) | ||
| NM_001207043.1:c.447G>C | NP_001193972.1:p.Pro149= | |
| NR_002139.2:n.489C>G (HCG4) | ||
| NR_132323.1:n.549G>C |