Linked Data
gnomAD v4:
5-55231649-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.55231649G>T , CM000667.2:g.55231649G>T | GRCh38 |
| NC_000005.9:g.54527477G>T , CM000667.1:g.54527477G>T | GRCh37 |
| NC_000005.8:g.54563234G>T | NCBI36 |
| NG_034201.1:g.7069C>A | |
| NG_051620.1:g.667C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282572.5:c.779C>A MANE Select | ENSP00000282572.4:p.Ala260Asp | |
| ENST00000282572.4:c.779C>A | ENSP00000282572.4:p.Ala260Asp | |
| ENST00000501463.2:c.*759C>A | ENSP00000422485.1:n.*759C>A | |
| NM_021147.4:c.779C>A | NP_066970.3:p.Ala260Asp | |
| NR_125346.1:n.1349C>A | ||
| NR_125347.1:n.978C>A | ||
| NR_125348.1:n.843C>A | ||
| NM_021147.5:c.779C>A MANE Select | NP_066970.3:p.Ala260Asp | |
| NR_125346.2:n.1240C>A | ||
| NR_125347.2:n.869C>A |