Linked Data
ClinVar Variation Id:
1562937
ClinVar RCV Id:
RCV002206751
dbSNP Id:
rs111477177
ExAC:
19:36398454 G / A
gnomAD v2:
19-36398454-G-A
gnomAD v3:
19-35907552-G-A
gnomAD v4:
19-35907552-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.35907552G>A , CM000681.2:g.35907552G>A | GRCh38 |
| NC_000019.9:g.36398454G>A , CM000681.1:g.36398454G>A | GRCh37 |
| NC_000019.8:g.41090294G>A | NCBI36 |
| NG_009304.1:g.5733C>T , LRG_607:g.5733C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262629.9:c.123C>T MANE Select | ENSP00000262629.3:p.Gly41= | |
| ENST00000262629.8:c.123C>T | ENSP00000262629.3:p.Gly41= | |
| ENST00000424586.7:c.90C>T | ENSP00000402371.3:p.Gly30= | |
| ENST00000544690.6:c.90C>T | ENSP00000445332.1:p.Gly30= | |
| ENST00000585626.1:n.190C>T | ||
| ENST00000585901.6:c.123C>T | ENSP00000468608.1:p.Gly41= | |
| ENST00000586946.1:c.*8C>T | ENSP00000465656.1:n.*8C>T | |
| ENST00000587837.5:c.*8C>T | ENSP00000465081.1:n.*8C>T | |
| ENST00000588439.1:n.267C>T | ||
| ENST00000589517.1:c.123C>T | ENSP00000468447.1:p.Gly41= | |
| NM_001173514.1:c.90C>T | NP_001166985.1:p.Gly30= | |
| NM_001173515.1:c.90C>T | NP_001166986.1:p.Gly30= | |
| NM_003332.3:c.123C>T , LRG_607t1:c.123C>T | NP_003323.1:p.Gly41= | |
| NM_198125.2:c.123C>T | NP_937758.1:p.Gly41= | |
| NR_033390.1:n.164C>T | ||
| NM_001173514.2:c.90C>T | NP_001166985.1:p.Gly30= | |
| NM_001173515.2:c.90C>T | NP_001166986.1:p.Gly30= | |
| NM_003332.4:c.123C>T MANE Select | NP_003323.1:p.Gly41= | |
| NM_198125.3:c.123C>T | NP_937758.1:p.Gly41= | |
| NR_033390.2:n.150C>T |