Linked Data
ClinVar Variation Id:
3183663
ClinVar RCV Id:
RCV004476480
dbSNP Id:
rs1891769304
gnomAD v4:
14-81143122-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.81143122T>C , CM000676.2:g.81143122T>C | GRCh38 |
| NC_000014.8:g.81609466T>C , CM000676.1:g.81609466T>C | GRCh37 |
| NC_000014.7:g.80679219T>C | NCBI36 |
| NG_009206.1:g.192598T>C , LRG_523:g.192598T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000298171.7:c.1064T>C MANE Select | ENSP00000298171.2:p.Phe355Ser | |
| ENST00000636454.1:n.982T>C | ||
| ENST00000298171.6:c.1064T>C | ENSP00000298171.2:p.Phe355Ser | |
| ENST00000541158.6:c.1064T>C | ENSP00000441235.2:p.Phe355Ser | |
| NM_000369.2:c.1064T>C , LRG_523t1:c.1064T>C | NP_000360.2:p.Phe355Ser | |
| XM_005268037.3:c.1064T>C | XP_005268094.1:p.Phe355Ser | |
| XM_011537119.1:c.785T>C | XP_011535421.1:p.Phe262Ser | |
| XR_245790.3:n.2086+22071A>G | ||
| XR_429385.2:n.853+22071A>G | ||
| XR_429386.2:n.854+22071A>G | ||
| XR_944075.1:n.865+22071A>G | ||
| XR_944076.1:n.861+22071A>G | ||
| XR_944077.1:n.865+22071A>G | ||
| XR_944078.1:n.865+22071A>G | ||
| XR_944079.1:n.855+22071A>G | ||
| XM_005268037.4:c.1064T>C | XP_005268094.1:p.Phe355Ser | |
| XM_011537119.2:c.785T>C | XP_011535421.1:p.Phe262Ser | |
| XR_001751021.1:n.2753+22071A>G | ||
| XR_001751022.1:n.2753+22071A>G | ||
| XR_001751023.1:n.2753+22071A>G | ||
| XR_944075.3:n.929+22071A>G | ||
| NM_000369.4:c.1064T>C | NP_000360.2:p.Phe355Ser | |
| NM_000369.5:c.1064T>C MANE Select | NP_000360.2:p.Phe355Ser |