Linked Data
ClinVar Variation Id:
2096364
ClinVar RCV Id:
RCV003028195
dbSNP Id:
rs2036350519
gnomAD v3:
14-24082636-C-T
gnomAD v4:
14-24082636-C-T
MyVariant Identifiers:
chr14:g.24551845C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.24082636C>T , CM000676.2:g.24082636C>T | GRCh38 |
| NC_000014.8:g.24551845C>T , CM000676.1:g.24551845C>T | GRCh37 |
| NC_000014.7:g.23621685C>T | NCBI36 |
| NG_011697.1:g.6988G>A | |
| NG_011697.2:g.37379G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000561028.6:c.213G>A MANE Select | ENSP00000454062.2:p.Glu71= | |
| ENST00000396997.1:c.213G>A | ENSP00000380193.1:p.Glu71= | |
| ENST00000397002.6:c.213G>A | ENSP00000380197.2:p.Glu71= | |
| ENST00000561028.5:c.213G>A | ENSP00000454062.1:p.Glu71= | |
| NM_006177.3:c.213G>A | NP_006168.1:p.Glu71= | |
| XM_005267708.3:c.213G>A | XP_005267765.1:p.Glu71= | |
| XM_005267709.3:c.213G>A | XP_005267766.1:p.Glu71= | |
| XM_005267710.3:c.213G>A | XP_005267767.1:p.Glu71= | |
| XM_011536801.1:c.312G>A | XP_011535103.1:p.Glu104= | |
| XM_011536802.1:c.213G>A | XP_011535104.1:p.Glu71= | |
| XM_011536803.1:c.213G>A | XP_011535105.1:p.Glu71= | |
| XM_011536804.1:c.213G>A | XP_011535106.1:p.Glu71= | |
| XM_011536805.1:c.213G>A | XP_011535107.1:p.Glu71= | |
| XM_011536806.1:c.165+147G>A | XP_011535108.1:n.165+147G>A | |
| NM_001354768.1:c.213G>A | NP_001341697.1:p.Glu71= | |
| NM_001354769.1:c.213G>A | NP_001341698.1:p.Glu71= | |
| NM_001354770.1:c.66+147G>A | NP_001341699.1:n.66+147G>A | |
| NM_006177.4:c.213G>A | NP_006168.1:p.Glu71= | |
| XM_011536801.2:c.519G>A | XP_011535103.2:p.Glu173= | |
| XM_011536804.2:c.213G>A | XP_011535106.1:p.Glu71= | |
| XM_011536805.2:c.213G>A | XP_011535107.1:p.Glu71= | |
| XM_011536806.2:c.372+147G>A | XP_011535108.2:n.372+147G>A | |
| NM_001354768.3:c.213G>A MANE Select | NP_001341697.1:p.Glu71= | |
| NM_001354770.2:c.66+147G>A | NP_001341699.1:n.66+147G>A | |
| NM_006177.5:c.213G>A | NP_006168.1:p.Glu71= |