Linked Data
gnomAD v4:
14-96204797-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.96204797C>G , CM000676.2:g.96204797C>G | GRCh38 |
| NC_000014.8:g.96671134C>G , CM000676.1:g.96671134C>G | GRCh37 |
| NC_000014.7:g.95740887C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000542454.2:c.-2970C>G | ENSP00000439459.2:n.-2970C>G | |
| ENST00000554311.1:c.-202C>G | ENSP00000450482.1:n.-202C>G |