Linked Data
gnomAD v4:
6-28161885-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.28161885C>T , CM000668.2:g.28161885C>T | GRCh38 |
| NC_000006.11:g.28129663C>T , CM000668.1:g.28129663C>T | GRCh37 |
| NC_000006.10:g.28237642C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000562227.2:n.53+64C>T | ||
| ENST00000440790.6:n.41+64C>T | ||
| ENST00000570126.1:n.30+64C>T | ||
| NR_103448.1:n.61+64C>T |