Linked Data
MyVariant Identifiers:
chr6:g.31362442A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31394665A>C , CM000668.2:g.31394665A>C | GRCh38 |
| NC_000006.11:g.31362442A>C , CM000668.1:g.31362442A>C | GRCh37 |
| NC_000006.10:g.31470421A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_241998.3:n.980T>G | ||
| NR_148222.1:n.970T>G | ||
| NR_148223.1:n.1003T>G |