Linked Data
MyVariant Identifiers:
chr6:g.32358301T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32390524T>G , CM000668.2:g.32390524T>G | GRCh38 |
| NC_000006.11:g.32358301T>G , CM000668.1:g.32358301T>G | GRCh37 |
| NC_000006.10:g.32466279T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_044996.1:n.15T>G (HCG23) | ||
| XM_011515039.1:c.482-14930T>G (TSBP1-AS1) | XP_011513341.1:n.482-14930T>G | |
| NR_136245.1:n.303-14930T>G (TSBP1-AS1) |