Linked Data
MyVariant Identifiers:
chr6:g.43965031T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.43997294T>C , CM000668.2:g.43997294T>C | GRCh38 |
| NC_000006.11:g.43965031T>C , CM000668.1:g.43965031T>C | GRCh37 |
| NC_000006.10:g.44073009T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_125864.1:n.661A>G (SCIRT) | ||
| NR_125865.1:n.445A>G (SCIRT) | ||
| NM_001318876.2:c.946-444596T>C (POLR1C) | NP_001305805.1:n.946-444596T>C |