Linked Data
gnomAD v4:
4-55346191-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.55346191G>T , CM000666.2:g.55346191G>T | GRCh38 |
| NC_000004.11:g.56212358G>T , CM000666.1:g.56212358G>T | GRCh37 |
| NC_000004.10:g.55907115G>T | NCBI36 |
| NG_028230.1:g.4971G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264228.8:c.-146G>T | ENSP00000264228.4:n.-146G>T |