Linked Data
ClinVar Variation Id:
1423596
ClinVar RCV Id:
RCV001928947
dbSNP Id:
rs370554511
ExAC:
9:130581021 C / G
gnomAD v2:
9-130581021-C-G
gnomAD v3:
9-127818742-C-G
gnomAD v4:
9-127818742-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.127818742C>G , CM000671.2:g.127818742C>G | GRCh38 |
| NC_000009.11:g.130581021C>G , CM000671.1:g.130581021C>G | GRCh37 |
| NC_000009.10:g.129620842C>G | NCBI36 |
| NG_009551.1:g.41027G>C , LRG_589:g.41027G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000480266.6:c.856G>C | ENSP00000479015.1:p.Glu286Gln | |
| ENST00000373203.9:c.1402G>C MANE Select | ENSP00000362299.4:p.Glu468Gln | |
| ENST00000344849.4:c.1402G>C | ENSP00000341917.3:p.Glu468Gln | |
| ENST00000373203.8:c.1402G>C | ENSP00000362299.4:p.Glu468Gln | |
| ENST00000480266.5:c.856G>C | ENSP00000479015.1:p.Glu286Gln | |
| NM_000118.3:c.1402G>C , LRG_589t1:c.1402G>C | NP_000109.1:p.Glu468Gln | |
| NM_001114753.2:c.1402G>C , LRG_589t2:c.1402G>C | NP_001108225.1:p.Glu468Gln | |
| NM_001278138.1:c.856G>C | NP_001265067.1:p.Glu286Gln | |
| NR_136302.1:n.1568+31C>G | ||
| NM_001114753.3:c.1402G>C MANE Select | NP_001108225.1:p.Glu468Gln | |
| NM_001278138.2:c.856G>C | NP_001265067.1:p.Glu286Gln |