Linked Data
ClinVar Variation Id:
3073636
ClinVar RCV Id:
RCV004016642
COSMIC:
COSM6060578
MyVariant Identifiers:
chr1:g.201044702C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.201075574C>A , CM000663.2:g.201075574C>A | GRCh38 |
| NC_000001.10:g.201044702C>A , CM000663.1:g.201044702C>A | GRCh37 |
| NC_000001.9:g.199311325C>A | NCBI36 |
| NG_009816.1:g.41993G>T | |
| NG_009816.2:g.41993G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000362061.4:c.1869G>T MANE Select | ENSP00000355192.3:p.Gly623= | |
| ENST00000679417.1:c.*1032G>T | ENSP00000506706.1:n.*1032G>T | |
| ENST00000680059.1:c.1869G>T | ENSP00000504944.1:p.Gly623= | |
| ENST00000681078.1:c.1869G>T | ENSP00000506645.1:p.Gly623= | |
| ENST00000681190.1:c.1869G>T | ENSP00000506428.1:p.Gly623= | |
| ENST00000681874.1:c.1869G>T | ENSP00000505162.1:p.Gly623= | |
| ENST00000362061.3:c.1869G>T | ENSP00000355192.3:p.Gly623= | |
| ENST00000367338.7:c.1869G>T | ENSP00000356307.3:p.Gly623= | |
| NM_000069.2:c.1869G>T | NP_000060.2:p.Gly623= | |
| XM_005245478.2:c.1869G>T | XP_005245535.1:p.Gly623= | |
| XM_005245478.3:c.1869G>T | XP_005245535.1:p.Gly623= | |
| NM_000069.3:c.1869G>T MANE Select | NP_000060.2:p.Gly623= |