Linked Data
gnomAD v4:
3-185254170-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.185254170C>T , CM000665.2:g.185254170C>T | GRCh38 |
| NC_000003.11:g.184971958C>T , CM000665.1:g.184971958C>T | GRCh37 |
| NC_000003.10:g.186454652C>T | NCBI36 |
| NG_015999.1:g.4929G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000465178.1:n.228-5653G>A | ||
| XM_011512517.1:c.-214-5653G>A | XP_011510819.1:n.-214-5653G>A |