Linked Data
ClinVar Variation Id:
135414
dbSNP Id:
rs139265251
ExAC:
X:48544175 G / A
gnomAD v2:
X-48544175-G-A
gnomAD v3:
X-48685786-G-A
gnomAD v4:
X-48685786-G-A
PubMed:
PMID:24728327
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.48685786G>A , CM000685.2:g.48685786G>A | GRCh38 |
| NC_000023.10:g.48544175G>A , CM000685.1:g.48544175G>A | GRCh37 |
| NC_000023.9:g.48429119G>A | NCBI36 |
| NG_007877.1:g.6990G>A , LRG_125:g.6990G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000483750.6:n.446G>A | ||
| ENST00000490627.2:n.25G>A | ||
| ENST00000698625.1:c.413G>A | ENSP00000513844.1:p.Arg138Gln | |
| ENST00000698626.1:c.413G>A | ENSP00000513845.1:p.Arg138Gln | |
| ENST00000698635.1:c.413G>A | ENSP00000513850.1:p.Arg138Gln | |
| ENST00000376701.5:c.413G>A MANE Select | ENSP00000365891.4:p.Arg138Gln | |
| ENST00000376701.4:c.413G>A | ENSP00000365891.4:p.Arg138Gln | |
| ENST00000450772.5:c.413G>A | ENSP00000410537.1:p.Arg138Gln | |
| ENST00000465982.5:n.448G>A | ||
| ENST00000483750.5:n.439G>A | ||
| ENST00000490627.1:n.8G>A | ||
| NM_000377.2:c.413G>A , LRG_125t1:c.413G>A | NP_000368.1:p.Arg138Gln | |
| XM_011543977.1:c.413G>A | XP_011542279.1:p.Arg138Gln | |
| XM_011543977.2:c.413G>A | XP_011542279.1:p.Arg138Gln | |
| XM_017029786.1:c.413G>A | XP_016885275.1:p.Arg138Gln | |
| NM_000377.3:c.413G>A MANE Select | NP_000368.1:p.Arg138Gln |