Linked Data
gnomAD v4:
5-55232914-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.55232914A>T , CM000667.2:g.55232914A>T | GRCh38 |
| NC_000005.9:g.54528742A>T , CM000667.1:g.54528742A>T | GRCh37 |
| NC_000005.8:g.54564499A>T | NCBI36 |
| NG_034201.1:g.5804T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282572.5:c.381+229T>A MANE Select | ENSP00000282572.4:n.381+229T>A | |
| ENST00000282572.4:c.381+229T>A | ENSP00000282572.4:n.381+229T>A | |
| ENST00000501463.2:c.*214T>A | ENSP00000422485.1:n.*214T>A | |
| NM_021147.4:c.381+229T>A | NP_066970.3:n.381+229T>A | |
| NR_125346.1:n.804T>A | ||
| NR_125347.1:n.580+224T>A | ||
| NR_125348.1:n.78T>A | ||
| NM_021147.5:c.381+229T>A MANE Select | NP_066970.3:n.381+229T>A | |
| NR_125346.2:n.695T>A | ||
| NR_125347.2:n.471+224T>A |