Linked Data
MyVariant Identifiers:
chr6:g.31245442T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31277665T>G , CM000668.2:g.31277665T>G | GRCh38 |
| NC_000006.11:g.31245442T>G , CM000668.1:g.31245442T>G | GRCh37 |
| NC_000006.10:g.31353421T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000494673.1:n.2094T>G |