Linked Data
gnomAD v4:
5-55233642-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.55233642G>T , CM000667.2:g.55233642G>T | GRCh38 |
| NC_000005.9:g.54529470G>T , CM000667.1:g.54529470G>T | GRCh37 |
| NC_000005.8:g.54565227G>T | NCBI36 |
| NG_034201.1:g.5076C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282572.4:c.-119C>A | ENSP00000282572.4:n.-119C>A | |
| NM_021147.4:c.-119C>A | NP_066970.3:n.-119C>A | |
| NR_125346.1:n.76C>A | ||
| NR_125347.1:n.76C>A |