Linked Data
gnomAD v4:
1-159714598-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.159714598C>T , CM000663.2:g.159714598C>T | GRCh38 |
| NC_000001.10:g.159684388C>T , CM000663.1:g.159684388C>T | GRCh37 |
| NC_000001.9:g.157951012C>T | NCBI36 |
| NG_013007.1:g.4992G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011509207.1:c.-113G>A | XP_011507509.1:n.-113G>A |