Linked Data
ClinVar Variation Id:
2121219
ClinVar RCV Id:
RCV003027935
MyVariant Identifiers:
chr1:g.40557770A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.40092098A>G , CM000663.2:g.40092098A>G | GRCh38 |
| NC_000001.10:g.40557770A>G , CM000663.1:g.40557770A>G | GRCh37 |
| NC_000001.9:g.40330357A>G | NCBI36 |
| NG_009192.1:g.10373T>C , LRG_690:g.10373T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372779.9:c.*145T>C | ENSP00000361865.5:n.*145T>C | |
| ENST00000433473.8:c.306T>C | ENSP00000394863.4:p.Pro102= | |
| ENST00000439754.6:c.309T>C | ENSP00000403207.2:p.Pro103= | |
| ENST00000449045.7:c.125-2586T>C | ENSP00000392293.2:n.125-2586T>C | |
| ENST00000526547.2:c.589T>C | ||
| ENST00000527311.7:c.234+300T>C | ENSP00000436695.3:n.234+300T>C | |
| ENST00000530704.6:c.309T>C | ENSP00000431655.1:p.Pro103= | |
| ENST00000641083.1:c.287T>C | ||
| ENST00000641236.1:n.546T>C | ||
| ENST00000641319.1:c.309T>C | ENSP00000493128.1:p.Pro103= | |
| ENST00000641471.1:c.396T>C | ENSP00000493146.1:p.Pro132= | |
| ENST00000641548.1:c.*161T>C | ENSP00000492984.1:n.*161T>C | |
| ENST00000641691.1:c.*161T>C | ENSP00000492910.1:n.*161T>C | |
| ENST00000641924.1:c.124+5017T>C | ENSP00000493063.1:n.124+5017T>C | |
| ENST00000642050.2:c.309T>C MANE Select | ENSP00000493153.1:p.Pro103= | |
| ENST00000372779.8:c.396T>C | ENSP00000361865.4:p.Pro132= | |
| ENST00000433473.7:c.309T>C | ENSP00000394863.3:p.Pro103= | |
| ENST00000449045.6:c.125-2586T>C | ENSP00000392293.2:n.125-2586T>C | |
| ENST00000526547.1:c.159T>C | ENSP00000436481.1:p.Pro53= | |
| ENST00000527311.6:c.125-41T>C | ENSP00000436695.2:n.125-41T>C | |
| ENST00000529905.5:c.309T>C | ENSP00000432053.1:p.Pro103= | |
| ENST00000530704.5:c.309T>C | ENSP00000431655.1:p.Pro103= | |
| NM_000310.3:c.309T>C , LRG_690t1:c.309T>C | NP_000301.1:p.Pro103= | |
| NM_001142604.1:c.125-2586T>C | NP_001136076.1:n.125-2586T>C | |
| XM_005271008.1:c.309T>C | XP_005271065.1:p.Pro103= | |
| NM_001363695.1:c.309T>C | NP_001350624.1:p.Pro103= | |
| NM_000310.4:c.309T>C MANE Select | NP_000301.1:p.Pro103= | |
| NM_001142604.2:c.125-2586T>C | NP_001136076.1:n.125-2586T>C | |
| NM_001363695.2:c.309T>C | NP_001350624.1:p.Pro103= |