Linked Data
MyVariant Identifiers:
chr6:g.31362519C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31394742C>G , CM000668.2:g.31394742C>G | GRCh38 |
| NC_000006.11:g.31362519C>G , CM000668.1:g.31362519C>G | GRCh37 |
| NC_000006.10:g.31470498C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_241998.3:n.903G>C | ||
| NR_148222.1:n.893G>C | ||
| NR_148223.1:n.926G>C |