Linked Data
MyVariant Identifiers:
chr6:g.31431705T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31463928T>C , CM000668.2:g.31463928T>C | GRCh38 |
| NC_000006.11:g.31431705T>C , CM000668.1:g.31431705T>C | GRCh37 |
| NC_000006.10:g.31539684T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_040662.1:n.658T>C |