Linked Data
ClinVar Variation Id:
196943
dbSNP Id:
rs200465274
ExAC:
14:21859651 C / T
gnomAD v2:
14-21859651-C-T
gnomAD v3:
14-21391492-C-T
gnomAD v4:
14-21391492-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.21391492C>T , CM000676.2:g.21391492C>T | GRCh38 |
| NC_000014.8:g.21859651C>T , CM000676.1:g.21859651C>T | GRCh37 |
| NC_000014.7:g.20929491C>T | NCBI36 |
| NG_021249.1:g.50807G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000430710.8:c.6199G>A | ENSP00000406288.3:p.Glu2067Lys | |
| ENST00000553870.2:c.437+341G>A | ||
| ENST00000555935.2:c.4736G>A | ||
| ENST00000557364.6:c.7036G>A | ENSP00000451601.1:p.Glu2346Lys | |
| ENST00000643469.1:c.7036G>A | ENSP00000495070.1:p.Glu2346Lys | |
| ENST00000645206.1:n.6192G>A | ||
| ENST00000645929.1:c.6199G>A | ENSP00000494402.1:p.Glu2067Lys | |
| ENST00000646647.2:c.7036G>A MANE Select | ENSP00000495240.1:p.Glu2346Lys | |
| ENST00000399982.6:c.7036G>A | ENSP00000382863.2:p.Glu2346Lys | |
| ENST00000430710.7:c.6199G>A | ENSP00000406288.3:p.Glu2067Lys | |
| ENST00000553870.1:c.396+341G>A | ENSP00000451071.1:n.396+341G>A | |
| ENST00000557364.5:c.7036G>A | ENSP00000451601.1:p.Glu2346Lys | |
| NM_001170629.1:c.7036G>A | NP_001164100.1:p.Glu2346Lys | |
| NM_020920.3:c.6199G>A | NP_065971.2:p.Glu2067Lys | |
| XR_001750627.1:n.704C>T | ||
| NM_001170629.2:c.7036G>A MANE Select | NP_001164100.1:p.Glu2346Lys | |
| NM_020920.4:c.6199G>A | NP_065971.2:p.Glu2067Lys |