Linked Data
gnomAD v4:
4-121697002-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.121697002A>T , CM000666.2:g.121697002A>T | GRCh38 |
| NC_000004.11:g.122618157A>T , CM000666.1:g.122618157A>T | GRCh37 |
| NC_000004.10:g.122837607A>T | NCBI36 |
| NG_032042.1:g.4991T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296511.9:c.-175T>A | ENSP00000296511.5:n.-175T>A |