Linked Data
dbSNP Id:
rs1448312194
gnomAD v4:
6-32390518-C-T
MyVariant Identifiers:
chr6:g.32358295C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32390518C>T , CM000668.2:g.32390518C>T | GRCh38 |
| NC_000006.11:g.32358295C>T , CM000668.1:g.32358295C>T | GRCh37 |
| NC_000006.10:g.32466273C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_044996.1:n.9C>T (HCG23) | ||
| XM_011515039.1:c.482-14936C>T (TSBP1-AS1) | XP_011513341.1:n.482-14936C>T | |
| NR_136245.1:n.303-14936C>T (TSBP1-AS1) |