Linked Data
gnomAD v4:
1-204190323-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.204190323C>T , CM000663.2:g.204190323C>T | GRCh38 |
| NC_000001.10:g.204159451C>T , CM000663.1:g.204159451C>T | GRCh37 |
| NC_000001.9:g.202426074C>T | NCBI36 |
| NG_032151.1:g.11169G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000638118.1:c.-302G>A | ENSP00000490307.1:n.-302G>A |