Linked Data
gnomAD v4:
6-112069732-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.112069732C>A , CM000668.2:g.112069732C>A | GRCh38 |
| NC_000006.11:g.112390935C>A , CM000668.1:g.112390935C>A | GRCh37 |
| NC_000006.10:g.112497628C>A | NCBI36 |
| NG_011748.1:g.20658C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361714.5:c.*112C>A | ENSP00000354734.2:n.*112C>A | |
| ENST00000368666.6:c.*112C>A | ENSP00000357655.3:n.*112C>A |