Linked Data
MyVariant Identifiers:
chr6:g.32358311G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32390534G>C , CM000668.2:g.32390534G>C | GRCh38 |
| NC_000006.11:g.32358311G>C , CM000668.1:g.32358311G>C | GRCh37 |
| NC_000006.10:g.32466289G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_044996.1:n.25G>C (HCG23) | ||
| XM_011515039.1:c.482-14920G>C (TSBP1-AS1) | XP_011513341.1:n.482-14920G>C | |
| NR_136245.1:n.303-14920G>C (TSBP1-AS1) |