Linked Data
gnomAD v4:
6-31969788-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31969788C>T , CM000668.2:g.31969788C>T | GRCh38 |
| NC_000006.11:g.31937565C>T , CM000668.1:g.31937565C>T | GRCh37 |
| NC_000006.10:g.32045544C>T | NCBI36 |
| NG_032652.1:g.15985C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461073.6:c.*2862C>T | ENSP00000419905.1:n.*2862C>T | |
| XR_926301.3:n.3830C>T |