Linked Data
gnomAD v4:
4-55346120-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.55346120A>C , CM000666.2:g.55346120A>C | GRCh38 |
| NC_000004.11:g.56212287A>C , CM000666.1:g.56212287A>C | GRCh37 |
| NC_000004.10:g.55907044A>C | NCBI36 |
| NG_028230.1:g.4900A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264228.8:c.-217A>C | ENSP00000264228.4:n.-217A>C |