Linked Data
gnomAD v4:
6-112069760-C-CTT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.112069763_112069764dup , CM000668.2:g.112069763_112069764dup | GRCh38 |
| NC_000006.11:g.112390966_112390967dup , CM000668.1:g.112390966_112390967dup | GRCh37 |
| NC_000006.10:g.112497659_112497660dup | NCBI36 |
| NG_011748.1:g.20689_20690dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361714.5:c.*143_*144dup | ENSP00000354734.2:n.*143_*144dup | |
| ENST00000368666.6:c.*143_*144dup | ENSP00000357655.3:n.*143_*144dup |