Linked Data
gnomAD v4:
4-121697076-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.121697076C>T , CM000666.2:g.121697076C>T | GRCh38 |
| NC_000004.11:g.122618231C>T , CM000666.1:g.122618231C>T | GRCh37 |
| NC_000004.10:g.122837681C>T | NCBI36 |
| NG_032042.1:g.4917G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296511.9:c.-249G>A | ENSP00000296511.5:n.-249G>A |