Linked Data
ClinVar Variation Id:
1723853
ClinVar RCV Id:
RCV002306414
dbSNP Id:
rs140829596
ExAC:
3:190122662 C / T
gnomAD v2:
3-190122662-C-T
gnomAD v3:
3-190404873-C-T
gnomAD v4:
3-190404873-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.190404873C>T , CM000665.2:g.190404873C>T | GRCh38 |
| NC_000003.11:g.190122662C>T , CM000665.1:g.190122662C>T | GRCh37 |
| NC_000003.10:g.191605356C>T | NCBI36 |
| NG_008149.1:g.21822C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264734.3:c.329C>T MANE Select | ENSP00000264734.3:p.Pro110Leu | |
| ENST00000456423.2:c.115-5030C>T | ENSP00000414136.2:n.115-5030C>T | |
| ENST00000264734.2:c.539C>T | ENSP00000264734.2:p.Pro180Leu | |
| ENST00000456423.1:c.325-5030C>T | ENSP00000414136.1:n.325-5030C>T | |
| ENST00000468220.1:n.521C>T | ||
| NM_006580.3:c.539C>T | NP_006571.1:p.Pro180Leu | |
| NM_001378492.1:c.329C>T | NP_001365421.1:p.Pro110Leu | |
| NM_001378493.1:c.329C>T | NP_001365422.1:p.Pro110Leu | |
| NM_006580.4:c.329C>T MANE Select | NP_006571.2:p.Pro110Leu |