Linked Data
MyVariant Identifiers:
chr6:g.28129559G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.28161781G>C , CM000668.2:g.28161781G>C | GRCh38 |
| NC_000006.11:g.28129559G>C , CM000668.1:g.28129559G>C | GRCh37 |
| NC_000006.10:g.28237538G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000562227.2:n.13G>C | ||
| ENST00000440790.6:n.1G>C | ||
| NR_103448.1:n.21G>C |