Linked Data
gnomAD v4:
4-55346128-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.55346128C>T , CM000666.2:g.55346128C>T | GRCh38 |
| NC_000004.11:g.56212295C>T , CM000666.1:g.56212295C>T | GRCh37 |
| NC_000004.10:g.55907052C>T | NCBI36 |
| NG_028230.1:g.4908C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264228.8:c.-209C>T | ENSP00000264228.4:n.-209C>T |