Linked Data
ClinVar Variation Id:
241666
dbSNP Id:
rs141687678
ExAC:
16:3646371 C / T
gnomAD v2:
16-3646371-C-T
gnomAD v3:
16-3596370-C-T
gnomAD v4:
16-3596370-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.3596370C>T , CM000678.2:g.3596370C>T | GRCh38 |
| NC_000016.9:g.3646371C>T , CM000678.1:g.3646371C>T | GRCh37 |
| NC_000016.8:g.3586372C>T | NCBI36 |
| NG_028123.1:g.20215G>A , LRG_503:g.20215G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000294008.4:c.1707G>A MANE Select | ENSP00000294008.3:p.Pro569= | |
| ENST00000294008.3:c.1707G>A | ENSP00000294008.3:p.Pro569= | |
| ENST00000466154.5:n.2928G>A | ||
| NM_032444.2:c.1707G>A , LRG_503t1:c.1707G>A | NP_115820.2:p.Pro569= | |
| XM_011522715.1:c.1707G>A | XP_011521017.1:p.Pro569= | |
| NM_032444.3:c.1707G>A | NP_115820.2:p.Pro569= | |
| XM_011522715.3:c.1707G>A | XP_011521017.1:p.Pro569= | |
| XM_017023775.2:c.885G>A | XP_016879264.1:p.Pro295= | |
| XM_024450471.1:c.1707G>A | XP_024306239.1:p.Pro569= | |
| NM_032444.4:c.1707G>A MANE Select | NP_115820.2:p.Pro569= |