Linked Data
MyVariant Identifiers:
chr6:g.26233372T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.26233144T>G , CM000668.2:g.26233144T>G | GRCh38 |
| NC_000006.11:g.26233372T>G , CM000668.1:g.26233372T>G | GRCh37 |
| NC_000006.10:g.26341351T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000403259.1:n.23T>G |