Linked Data
gnomAD v4:
11-5234662-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5234662C>A , CM000673.2:g.5234662C>A | GRCh38 |
| NC_000011.9:g.5255892C>A , CM000673.1:g.5255892C>A | GRCh37 |
| NC_000011.8:g.5212468C>A | NCBI36 |
| NG_000007.3:g.62954G>T | |
| NG_063112.2:g.13996G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000643122.1:c.-28-201G>T | ENSP00000494708.1:n.-28-201G>T | |
| ENST00000429817.1:c.-97-132G>T | ENSP00000393810.1:n.-97-132G>T |