Linked Data
ClinVar Variation Id:
21395
dbSNP Id:
rs113994090
ExAC:
2:29446307 G / A
gnomAD v2:
2-29446307-G-A
gnomAD v3:
2-29223441-G-A
gnomAD v4:
2-29223441-G-A
PubMed:
PMID:20301782
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29223441G>A , CM000664.2:g.29223441G>A | GRCh38 |
| NC_000002.11:g.29446307G>A , CM000664.1:g.29446307G>A | GRCh37 |
| NC_000002.10:g.29299811G>A | NCBI36 |
| NG_009445.1:g.703126C>T , LRG_488:g.703126C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389048.8:c.3260C>T MANE Select | ENSP00000373700.3:p.Thr1087Ile | |
| ENST00000431873.6:c.487C>T | ||
| ENST00000638605.1:n.137C>T | ||
| ENST00000642122.1:c.56C>T | ENSP00000493203.1:p.Thr19Ile | |
| ENST00000389048.7:c.3260C>T | ENSP00000373700.3:p.Thr1087Ile | |
| ENST00000431873.5:c.140C>T | ENSP00000414027.2:p.Thr47Ile | |
| ENST00000618119.4:c.2129C>T | ENSP00000482733.1:p.Thr710Ile | |
| NM_004304.4:c.3260C>T | NP_004295.2:p.Thr1087Ile | |
| NM_001353765.1:c.56C>T | NP_001340694.1:p.Thr19Ile | |
| XM_024452778.1:c.413C>T | XP_024308546.1:p.Thr138Ile | |
| XM_024452779.1:c.56C>T | XP_024308547.1:p.Thr19Ile | |
| NM_004304.5:c.3260C>T MANE Select | NP_004295.2:p.Thr1087Ile | |
| NM_001353765.2:c.56C>T | NP_001340694.1:p.Thr19Ile |