Linked Data
gnomAD v4:
4-121697093-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.121697093T>G , CM000666.2:g.121697093T>G | GRCh38 |
| NC_000004.11:g.122618248T>G , CM000666.1:g.122618248T>G | GRCh37 |
| NC_000004.10:g.122837698T>G | NCBI36 |
| NG_032042.1:g.4900A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296511.9:c.-266A>C | ENSP00000296511.5:n.-266A>C |