Linked Data
ClinVar Variation Id:
796475
ClinVar RCV Id:
RCV000979864
dbSNP Id:
rs183509078
ExAC:
1:209807954 C / T
gnomAD v2:
1-209807954-C-T
gnomAD v3:
1-209634609-C-T
gnomAD v4:
1-209634609-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.209634609C>T , CM000663.2:g.209634609C>T | GRCh38 |
| NC_000001.10:g.209807954C>T , CM000663.1:g.209807954C>T | GRCh37 |
| NC_000001.9:g.207874577C>T | NCBI36 |
| NG_007116.1:g.22867G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356082.9:c.402G>A MANE Select | ENSP00000348384.3:p.Glu134= | |
| ENST00000356082.8:c.402G>A | ENSP00000348384.3:p.Glu134= | |
| ENST00000367030.7:c.402G>A | ENSP00000355997.3:p.Glu134= | |
| ENST00000391911.5:c.402G>A | ENSP00000375778.1:p.Glu134= | |
| ENST00000415782.1:c.402G>A | ENSP00000388960.1:p.Glu134= | |
| NM_000228.2:c.402G>A | NP_000219.2:p.Glu134= | |
| NM_001017402.1:c.402G>A | NP_001017402.1:p.Glu134= | |
| NM_001127641.1:c.402G>A | NP_001121113.1:p.Glu134= | |
| XM_005273124.3:c.402G>A | XP_005273181.1:p.Glu134= | |
| XM_005273124.4:c.402G>A | XP_005273181.1:p.Glu134= | |
| XM_017001272.2:c.373-1476G>A | XP_016856761.1:n.373-1476G>A | |
| NM_000228.3:c.402G>A MANE Select | NP_000219.2:p.Glu134= | |
| NM_001017402.2:c.402G>A | NP_001017402.1:p.Glu134= |