Linked Data
ClinVar Variation Id:
56025
ClinVar RCV Id:
RCV000049434
dbSNP Id:
rs386833506
gnomAD v4:
5-149978148-G-A
PubMed:
PMID:11241838
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149978148G>A , CM000667.2:g.149978148G>A | GRCh38 |
| NC_000005.9:g.149357711G>A , CM000667.1:g.149357711G>A | GRCh37 |
| NC_000005.8:g.149337904G>A | NCBI36 |
| NG_007147.2:g.19266G>A , LRG_684:g.19266G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000690410.1:n.728G>A | ||
| ENST00000286298.5:c.496G>A MANE Select | ENSP00000286298.4:p.Gly166Arg | |
| ENST00000286298.4:c.496G>A | ENSP00000286298.4:p.Gly166Arg | |
| ENST00000503336.1:c.169G>A | ENSP00000426053.1:p.Gly57Arg | |
| NM_000112.3:c.496G>A , LRG_684t1:c.496G>A | NP_000103.2:p.Gly166Arg | |
| XM_017009191.2:c.496G>A | XP_016864680.1:p.Gly166Arg | |
| NM_000112.4:c.496G>A MANE Select | NP_000103.2:p.Gly166Arg |