Linked Data
ClinVar Variation Id:
1670101
ClinVar RCV Id:
RCV002201280
dbSNP Id:
rs2124487917
gnomAD v4:
1-40092137-G-A
MyVariant Identifiers:
chr1:g.40557809G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.40092137G>A , CM000663.2:g.40092137G>A | GRCh38 |
| NC_000001.10:g.40557809G>A , CM000663.1:g.40557809G>A | GRCh37 |
| NC_000001.9:g.40330396G>A | NCBI36 |
| NG_009192.1:g.10334C>T , LRG_690:g.10334C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372779.9:c.*106C>T | ENSP00000361865.5:n.*106C>T | |
| ENST00000433473.8:c.267C>T | ENSP00000394863.4:p.Ser89= | |
| ENST00000439754.6:c.270C>T | ENSP00000403207.2:p.Ser90= | |
| ENST00000449045.7:c.125-2625C>T | ENSP00000392293.2:n.125-2625C>T | |
| ENST00000526547.2:c.550C>T | ||
| ENST00000527311.7:c.234+261C>T | ENSP00000436695.3:n.234+261C>T | |
| ENST00000530704.6:c.270C>T | ENSP00000431655.1:p.Ser90= | |
| ENST00000641083.1:c.248C>T | ||
| ENST00000641236.1:n.507C>T | ||
| ENST00000641319.1:c.270C>T | ENSP00000493128.1:p.Ser90= | |
| ENST00000641471.1:c.357C>T | ENSP00000493146.1:p.Ser119= | |
| ENST00000641548.1:c.*122C>T | ENSP00000492984.1:n.*122C>T | |
| ENST00000641691.1:c.*122C>T | ENSP00000492910.1:n.*122C>T | |
| ENST00000641924.1:c.124+4978C>T | ENSP00000493063.1:n.124+4978C>T | |
| ENST00000642050.2:c.270C>T MANE Select | ENSP00000493153.1:p.Ser90= | |
| ENST00000372779.8:c.357C>T | ENSP00000361865.4:p.Ser119= | |
| ENST00000433473.7:c.270C>T | ENSP00000394863.3:p.Ser90= | |
| ENST00000449045.6:c.125-2625C>T | ENSP00000392293.2:n.125-2625C>T | |
| ENST00000526547.1:c.120C>T | ENSP00000436481.1:p.Ser40= | |
| ENST00000527311.6:c.125-80C>T | ENSP00000436695.2:n.125-80C>T | |
| ENST00000529905.5:c.270C>T | ENSP00000432053.1:p.Ser90= | |
| ENST00000530704.5:c.270C>T | ENSP00000431655.1:p.Ser90= | |
| NM_000310.3:c.270C>T , LRG_690t1:c.270C>T | NP_000301.1:p.Ser90= | |
| NM_001142604.1:c.125-2625C>T | NP_001136076.1:n.125-2625C>T | |
| XM_005271008.1:c.270C>T | XP_005271065.1:p.Ser90= | |
| NM_001363695.1:c.270C>T | NP_001350624.1:p.Ser90= | |
| NM_000310.4:c.270C>T MANE Select | NP_000301.1:p.Ser90= | |
| NM_001142604.2:c.125-2625C>T | NP_001136076.1:n.125-2625C>T | |
| NM_001363695.2:c.270C>T | NP_001350624.1:p.Ser90= |