MyVariant.info:
GRCh37
chr6:g.32358513G>C
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32390736G>C , CM000668.2:g.32390736G>C | GRCh38 |
| NC_000006.11:g.32358513G>C , CM000668.1:g.32358513G>C | GRCh37 |
| NC_000006.10:g.32466491G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_044996.1:n.227G>C (HCG23) | ||
| XM_011515039.1:c.482-14718G>C (TSBP1-AS1) | XP_011513341.1:n.482-14718G>C | |
| NR_136245.1:n.303-14718G>C (TSBP1-AS1) |