Linked Data
gnomAD v4:
16-2340829-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2340829C>A , CM000678.2:g.2340829C>A | GRCh38 |
| NC_000016.9:g.2390830C>A , CM000678.1:g.2390830C>A | GRCh37 |
| NC_000016.8:g.2330831C>A | NCBI36 |
| NG_011790.1:g.4918G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000640929.1:n.42+1498C>A | ||
| ENST00000512848.5:n.182+1498C>A |