Linked Data
ClinVar Variation Id:
181290
dbSNP Id:
rs397516253
ExAC:
14:23883032 C / T
gnomAD v2:
14-23883032-C-T
gnomAD v4:
14-23413823-C-T
COSMIC:
COSM5694643
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23413823C>T , CM000676.2:g.23413823C>T | GRCh38 |
| NC_000014.8:g.23883032C>T , CM000676.1:g.23883032C>T | GRCh37 |
| NC_000014.7:g.22952872C>T | NCBI36 |
| NG_007884.1:g.26839G>A , LRG_384:g.26839G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000355349.4:c.5726G>A MANE Select | ENSP00000347507.3:p.Arg1909Gln | |
| ENST00000355349.3:c.5726G>A | ENSP00000347507.3:p.Arg1909Gln | |
| NM_000257.3:c.5726G>A | NP_000248.2:p.Arg1909Gln | |
| XM_017021340.1:c.5726G>A | XP_016876829.1:p.Arg1909Gln | |
| NM_000257.4:c.5726G>A MANE Select | NP_000248.2:p.Arg1909Gln |