Linked Data
ClinVar Variation Id:
2846379
ClinVar RCV Id:
RCV003757703
MyVariant Identifiers:
chr1:g.245027352C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.244864050C>T , CM000663.2:g.244864050C>T | GRCh38 |
| NC_000001.10:g.245027352C>T , CM000663.1:g.245027352C>T | GRCh37 |
| NC_000001.9:g.243093975C>T | NCBI36 |
| NG_042184.1:g.5476G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000283179.14:c.258G>A | ENSP00000283179.10:p.Glu86= | |
| ENST00000444376.7:c.258G>A | ENSP00000393151.2:p.Glu86= | |
| ENST00000476241.2:n.443G>A | ||
| ENST00000638475.1:c.42G>A | ENSP00000491305.1:p.Glu14= | |
| ENST00000638952.1:n.489G>A | ||
| ENST00000640218.2:c.258G>A MANE Select | ENSP00000491215.1:p.Glu86= | |
| ENST00000640306.1:c.258G>A | ENSP00000491685.1:p.Glu86= | |
| ENST00000649899.1:n.482G>A | ||
| ENST00000283179.13:c.258G>A | ENSP00000283179.9:p.Glu86= | |
| ENST00000444376.6:c.258G>A | ENSP00000393151.2:p.Glu86= | |
| ENST00000476241.1:n.442G>A | ||
| NM_004501.3:c.258G>A | NP_004492.2:p.Glu86= | |
| NM_031844.2:c.258G>A | NP_114032.2:p.Glu86= | |
| NM_031844.3:c.258G>A MANE Select | NP_114032.2:p.Glu86= |