Linked Data
MyVariant Identifiers:
chr6:g.26233371T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.26233143T>C , CM000668.2:g.26233143T>C | GRCh38 |
| NC_000006.11:g.26233371T>C , CM000668.1:g.26233371T>C | GRCh37 |
| NC_000006.10:g.26341350T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000403259.1:n.22T>C |