Linked Data
gnomAD v4:
19-3595576-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.3595576C>T , CM000681.2:g.3595576C>T | GRCh38 |
| NC_000019.9:g.3595574C>T , CM000681.1:g.3595574C>T | GRCh37 |
| NC_000019.8:g.3546574C>T | NCBI36 |
| NG_013363.1:g.16258G>A , LRG_578:g.16258G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375190.10:c.*112G>A MANE Select | ENSP00000364336.4:n.*112G>A | |
| ENST00000375190.8:c.*112G>A | ENSP00000364336.3:n.*112G>A | |
| ENST00000411851.3:c.983+161G>A | ENSP00000393333.2:n.983+161G>A | |
| ENST00000589966.1:c.755G>A | ENSP00000468145.1:p.Gly252Asp | |
| NM_001060.5:c.*112G>A , LRG_578t1:c.*112G>A | NP_001051.1:n.*112G>A | |
| NM_201636.2:c.983+161G>A | NP_963998.2:n.983+161G>A | |
| NM_001060.6:c.*112G>A MANE Select | NP_001051.1:n.*112G>A | |
| NM_201636.3:c.983+161G>A | NP_963998.2:n.983+161G>A |