Linked Data
gnomAD v4:
19-45767007-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.45767007A>T , CM000681.2:g.45767007A>T | GRCh38 |
| NC_000019.9:g.46270265A>T , CM000681.1:g.46270265A>T | GRCh37 |
| NC_000019.8:g.50962105A>T | NCBI36 |
| NG_012745.1:g.7233T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000317578.7:c.952T>A MANE Select | ENSP00000316842.4:p.Ser318Thr | |
| ENST00000317578.6:c.952T>A | ENSP00000316842.4:p.Ser318Thr | |
| ENST00000560160.1:c.587-896T>A | ||
| ENST00000560168.1:c.*140T>A | ENSP00000453189.2:n.*140T>A | |
| ENST00000622857.1:c.16-1045T>A | ENSP00000481365.1:n.16-1045T>A | |
| NM_175875.4:c.952T>A | NP_787071.2:p.Ser318Thr | |
| NM_175875.5:c.952T>A MANE Select | NP_787071.3:p.Ser318Thr |